Population genetics of Ice Age brown bears

The Pleistocene was a dynamic period for Holarctic mammal species, complicated by episodes of glaciation, local extinctions, and intercontinental migration. The genetic consequences of these events are difficult to resolve from the study of present-day populations. To provide a direct view of population genetics in the late Pleistocene, we measured mitochondrial DNA sequence variation in seven permafrost-preserved brown bear (Ursus arctos) specimens, dated from 14,000 to 42,000 years ago. Approximately 36,000 years ago, the Beringian brown bear population had a higher genetic diversity than any extant North American population, but by 15,000 years ago genetic diversity appears similar to the modern day. The older, genetically diverse, Beringian population contained sequences from three clades now restricted to local regions within North America, indicating that current phylogeographic patterns may provide misleading data for evolutionary studies and conservation management. The late Pleistocene phylogeographic data also indicate possible colonization routes to areas south of the Cordilleran ice sheet.

(Table 1) Neutral and phenolic organohalogen compounds in blubber samples of ringed seals (Pusa hispida) from East Greenland

We report on the comparative bioaccumulation, biotransformation and/or biomagnification from East Greenland ringed seal (Pusa hispida) blubber to polar bear (Ursus maritimus) tissues (adipose, liver and brain) of various classes and congeners of persistent chlorinated and brominated contaminants and metabolic by-products: polychlorinated biphenyls (PCBs), chlordanes (CHLs), hydroxyl (OH-) and methylsulfonyl (MeSO2-) PCBs, polybrominated biphenyls (PBBs), OH-PBBs, polybrominated diphenyl ether (PBDE) and hexabromocyclododecane (HBCD) flame retardants and OH- and methoxyl (MeO-) PBDEs, 2,2-dichloro-bis(4-chlorophenyl)ethene (p,p'-DDE), 3-MeSO2-p,p'-DDE, pentachlorophenol (PCP) and 4-OH-heptachlorostyrene (4-OH-HpCS). We detected all of the investigated contaminants in ringed seal blubber with high frequency, the main diet of East Greenland bears, with the exception of OH-PCBs and 4-OH-HpCS, which indicated that these phenolic contaminants were likely of metabolic origin and formed in the bears from accumulated PCBs and octachlorostyrene (OCS), respectively, rather than being bioaccumulated from a seal blubber diet. For all of the detectable sum of classes or individual organohalogens, in general, the ringed seal to polar bear mean BMFs for SumPCBs, p,p'-DDE, SumCHLs, SumMeSO2-PCBs, 3-MeSO2-p,p'-DDE, PCP, SumPBDEs, total-(alpha)-HBCD, SumOH-PBDEs, SumMeO-PBDEs and SumOH-PBBs indicated that these organohalogens bioaccumulate, and in some cases there was tissue-specific biomagnification, e.g., BMFs for bear adipose and liver ranged from 2 to 570. The blood-brain barrier appeared to be effective in minimizing brain accumulation as BMFs were <= 1 in the brain, with the exception of SumOH-PBBs (mean BMF = 93±54). Unlike OH-PCB metabolites, OH-PBDEs in the bear tissues appeared to be mainly accumulated from the seal blubber rather than being metabolic formed from PBDEs in the bears. In vitro PBDE depletion assays using polar bear hepatic microsomes, wherein the rate of oxidative metabolism of PBDE congeners was very slow, supported the probability that accumulation from seals is the main source of OH-PBDEs in the bear tissues. Our findings demonstrated from ringed seal to polar bears that organohalogen biotransformation, bioaccumulation and/or biomagnification varied widely and depended on the contaminant in question. Our results show the increasing complexity of bioaccumulated and in some cases biomagnified, chlorinated and brominated contaminants and/or metabolites from the diet may be a contributing stress factor in the health of East Greenland polar bears.

(Table 1) Organohalogen contaminants in adipose tissue of captive sledge dogs (Canis familiaris) fed with whale blubber or pork fat

Studies on the fate of organohalogen contaminants (OHCs) in wild top predator mammals in the Arctic have often been a challenge due to important knowledge deficiencies in the life history of the sampled animals. The present study investigated the influence of age, dietary and trans-generational factors on the fate of major lipophilic chlorinated and brominated OHCs in adipose tissue of a potential surrogate captive species for the polar bear (Ursus maritimus), the sledge dog (Canis familiaris) in West Greenland. Adult female sledge dogs (P) and their sexually-mature (F1) and/or pre-weaning pups (F1-MLK) were divided into an exposed group (EXP) fed blubber from a Greenland minke whale (Balaenoptera acutorostrata) and a control group (CON) given commercially available pork fat. Large dietary treatment-related differences in summed and individual congener/compound adipose tissue concentrations of polybrominated diphenyl ethers (PBDEs), hexachlorobenzene (HCB), chlordanes (CHLs) and polychlorinated biphenyls (PCBs) were found between the EXP and CON groups for all the sledge dog cohorts. However, among the F1-MLK, F1 and P dogs in both of the EXP and CON groups, little or no difference existed in PBDE, HCB, CHL and PCB concentrations, suggesting higher state of equilibrium in adipose tissue concentrations from a very early stage of life. In contrast, the distribution pattern (proportions to the summed concentrations) of OHC classes, and the major congeners/ compounds constituting those classes, varied on a dietary group- and/or cohort-dependent manner. The present captive sledge dog study demonstrated the importance of the confounding effects of diet composition, mother-pup association (maternal transfer), reproductive status (nursing), and to a lesser extent age in the fate of OHCs in adipose tissue of a large top carnivore mammal.

Body measurements and blood plasma lipid, PCB and OH-PCB content of polar bear (U. maritimus) mothers and cubs, Svalbard

The aim of this study was to examine the plasma concentrations and prevalence of polychlorinated biphenyls (PCBs) and hydroxylated PCB-metabolites (OH-PCBs) in polar bear (Ursus maritimus) mothers (n = 26) and their 4 months old cubs-of-the-year (n = 38) from Svalbard to gain insight into the mother-cub transfer, biotransformation and to evaluate the health risk associated with the exposure to these contaminants. As samplings were performed in 1997/1998 and 2008, we further investigated the differences in levels and pattern of PCBs between the two sampling years. The plasma concentrations of Sum(21)PCBs (1997/1998: 5710 ± 3090 ng/g lipid weight [lw], 2008: 2560±1500 ng/g lw) and Sum(6)OH-PCBs (1997/1998: 228 ± 60 ng/g wet weight [ww], 2008: 80 ± 38 ng/g ww) in mothers were significantly lower in 2008 compared to in 1997/1998. In cubs, the plasma concentrations of Sum(21)PCBs (1997/1998: 14680 ± 5350 ng/g lw, 2008: 6070 ± 2590 ng/g lw) and Sum(6)OH-PCBs (1997/1998: 98 ± 23 ng/g ww, 2008: 49 ± 21 ng/g ww) were also significantly lower in 2008 than in 1997/1998. Sum(21)PCBs in cubs was 2.7 ± 0.7 times higher than in their mothers. This is due to a significant maternal transfer of these contaminants. In contrast, Sum(6)OH-PCBs in cubs were approximately 0.53 ± 0.16 times the concentration in their mothers. This indicates a lower maternal transfer of OH-PCBs compared to PCBs. The majority of the metabolite/precursor-ratios were lower in cubs compared to mothers. This may indicate that cubs have a lower endogenous capacity to biotransform PCBs to OH-PCBs than polar bear mothers. Exposure to PCBs and OH-PCBs is a potential health risk for polar bears, and the levels of PCBs and OH-PCBs in cubs from 2008 were still above levels associated with health effects in humans and wildlife.

Impact des changements climatiques sur certaines espèces à statut précaire au Québec et analyse des mesures de protection actuelles

Le climat planétaire évolue à une vitesse alarmante. Selon le Groupe d’experts intergouvernemental sur l’évolution du climat, les températures globales pourraient grimper de 3 à 7°C d’ici 2100. Les zones tempérées, comme le Québec, ne seront pas épargnées. Au sein de la province, le climat typique en forêt boréale pourrait se déplacer de 750 km vers le nord pour atteindre le Haut-Arctique dans quelques décennies. D’autres modifications notables du climat se traduisent dans les précipitations, les glaces, les océans, etc. Tous ces changements climatiques constituent une menace grandissante pour la biodiversité. D’ailleurs, ils pourraient devenir la principale cause d’extinction d’espèces dans le futur, surpassant même la dégradation d’habitats et la pollution. Afin de témoigner de la portée des changements climatiques sur la biodiversité, 6 espèces fauniques à statut précaire au Québec sont étudiées dans le cadre de l’essai. Par leurs fortes réponses aux stress, elles agissent à titre de bioindicateurs des changements climatiques. Ces espèces, de classes taxonomiques différentes, sont : le chevalier cuivré (Moxostoma hubbsi), l’ours blanc (Ursus maritimus), la grive de Bicknell (Catharus Bicknelli), la rainette faux-grillon de l’Ouest (Pseudacris triseriata), la tortue luth (Dermochelys coriacea) et le satyre fauve des Maritimes (Coenonympha nipisiquit). L’étude approfondie de ces espèces a permis de relever un total de 47 impacts potentiels des changements climatiques. En majorité, ces impacts concernent la perte d’habitats, l’augmentation de la compétition, la diminution du succès reproducteur et l’entrave à la survie. L’objectif de cet essai est d’évaluer les mesures de protection actuelles permettant de faire face à ces impacts. Bien qu’elles varient grandement d’une espèce à l’autre, elles peuvent être regroupées en quatre grandes thématiques, soit la recherche et le suivi, la gestion des aires protégées, l’adaptation du cadre législatif et l’aménagement écosystémique. L’évaluation de ces mesures a permis de soulever certains constats. En premier lieu, la recherche et le suivi constituent la principale mesure de protection adoptée. En second lieu, il appert que les mesures de protection actuelles manquent de spécificité. En effet, dans la majorité des cas, elles protègent l’espèce de manière indirecte seulement. Au final, dans le but d’améliorer ou de combler les lacunes des mesures de protection actuelles, des recommandations ont été formulées. D’une part, celles-ci présentent des actions concrètes comme la translocation ou l’aménagement écosystémique. D’autre part, elles suggèrent des modifications quant aux méthodes de suivi, à la gestion des aires protégées et aux cadres législatifs.

Die cromerzeitlichen Bären aus der Einhornhöhle bei Scharzfeld

Up to now the bear remains from the "Einhornhöhle,, Cave near Scharzfeld at the foot of the Harz Mountains have been aseribed to the species "Ursus spelaeus" without undertaking comprehensive studies. Owing to an erroneous Classification of the gravel deposits covering part of the cave floor into the Middle Terrace of the Oder Rivulet, the fossil-bearing strata have been assigned to the Eemian Interglacial. RODE, who included a part of the Scharzfeld teeth in his treatise on teeth of the bears, has stated arctoidal features in their formation apart from certain specializations. He arrived at the conclusion that the Scharzfeld Bear differs more pronouncedly from all Central European Cave Bears he had investigated than the same differ from each other, and he named the Scharzfeld Bear: "Ursus spelaeus var. hercynica". The geological exploration of the Einhornhöhle Cave and of its environs carried out by DUPHORN in 196? resulted in the aforesaid gravels pertaining to a terrace of a Pre-Elster- Glaciation age; according to DUPHORN the fossil-bearing Sediments were deposited in a Pre-Elster-Glaciation ffarm- Climate Period. The very sparse aceompanying fauna does not contain any Stratigraphie key form; arctic elements and members of an interglacial forest fauna are missing. Its composition teils in favour of a dry, yet not too cool period of the Pleistocene, which is younger than the Villa- franchium. Consequently the cave must have been taken pos- session of for settling in the Cromerian Interglacial. The investigation of the bear remains has led to the result that, in all systematically .important teeth and skeleton characteristics, the Scharzfeld Bear shows either concor- dance with Ursus deningeri or greater analogy to the same than to Ursus spelaeus; in a few properties it even appears somewhat more primitive than Ursus deningeri. Therefore the bears of the Einhornhöhle Cave belong to the species "Ursus deningeri v. REICHENAU 1906". In the frontal teeth certain specializations occur. However, in view to the great varia- bility of the deningeri-"rassenkreis" there does not seem to be a justification for establishing a subspecies of its own. Whereas up to now nothing had been known in respect of the hibernation habits of Ursus deningeri, there has for the first time been furnished proof that an Ursus deningeri population had oecologically become "cave" bears. Consequently this specialization, as the onset and cause of which the Elster Glaciation was up to now considered, must already be originating in older cold epochs.

Reindeer habitat selection under the risk of brown bear predation during calving season

The depredation of semi-domesticated reindeer by large carnivores reflects an important human-wildlife conflict in Fennoscandia. Recent studies have revealed that brown bears (Ursus arctos) may kill substantial numbers of reindeer calves (Rangifer tarandus tarandus) in forest areas in Sweden. Several authors have suggested that predation risk is an important driver of habitat selection in wild Rangifer populations where predation is a limiting factor, but little is known about these mechanisms in semi-domesticated populations. We examined the habitat selection of female reindeer in relation to spatial and temporal variations in brown bear predation risk on the reindeer calving grounds and evaluated the simultaneous responses of brown bears and reindeer to landscape characteristics. We used GPS data from 110 reindeer years (97 individuals) and 29 brown bear years (19 individuals), from two reindeer herding districts in the forest area of northern Sweden. Our results did not indicate that reindeer alter their behavior in response to spatiotemporal variation in brown bear predation risk, on the scale of the calving range. Instead, we suggest that spatiotemporal behavioral adjustments by brown bears were the main driver of prey-predator interactions in our study system. Contrasting responses by brown bears and reindeer to clear-cuts and young forest indicate that forestry can influence species interactions and possibly yield negative consequences for the reindeer herd. Even if clear-cuts may be beneficial in terms of calf survival, logging activity will eventually cause greater abundance of young regenerating forest, reducing available reindeer habitats and increasing habitat preferred by brown bears. Domestication may have made semi-domesticated reindeer in Fennoscandia less adapted to cope with predators. Areal restrictions, limiting the opportunity for dispersion and escape, possibly make the calves more susceptible to predation. Also, a generally higher population density in semi-domesticated herds compared to wild populations can make dispersion a less efficient strategy and the reindeer calves easier prey. Overall, the lack of ability of the reindeer females to reduce brown bear encounter risk on the scale of the calving range is probably an important reason for the high brown bear predation rates on reindeer calves documented in our study areas.