Estimating population growth of grizzly bears from the Flathead River drainage using computer simulations of reproduction and survival rates

1996 ◽  
Vol 74 (8) ◽  
pp. 1409-1416 ◽  
Author(s):  
Frederick W. Hovey ◽  
Bruce N. McLellan
Keyword(s):  
Ursus Arctos ◽  
Survival Rates ◽  
Population Increase ◽  
Grizzly Bears ◽  
Grizzly Bear ◽  
Reproduction Rate ◽  
River Drainage ◽  
The North ◽  
Flathead River ◽  
Subadult Female

Using survival and reproduction data obtained from radio-tracking 23 adult female, 24 subadult female, 49 yearling, and 44 cub grizzly bears (Ursus arctos) in the Flathead River drainage of British Columbia and Montana, we estimated the finite rate of population increase [Formula: see text] from 1979 to 1994 at 1.085 ± 0.026, with ≈95% confidence limits of 1.032–1.136. Estimated annual survival rates were 0.946 ± 0.026 for adult females, 0.931 ± 0.038 for subadult females, 0.944 ± 0.039 for yearlings, and 0.867 ± 0.050 for cubs (rates for cubs and yearlings represented both sexes). The estimated annual reproduction rate and age at first parturition were 0.422 ± 0.042 female cubs per female and 6.44 ± 0.45 years, respectively. We found that uncertainty in [Formula: see text] was mostly attributable to uncertainty in survival rates (76.7%), with subadult (47.5%) and adult (21.9%) survival contributing the largest portions. These results indicated that to reduce uncertainty in [Formula: see text], further research on grizzly bears in our study area should focus on improving estimates of adult and subadult female survivorship. Other demographic variables are not as important in estimating the grizzly bear population trend in the North Fork of the Flathead River drainage.

scholarly journals Gray Wolf Prey Base Ecology in the North Fork of the Flathead River Drainage

1991 ◽  
Vol 15 ◽  
pp. 103-104
Author(s):  
C. Marcum ◽  
Daniel Pletscher ◽  
Michael Bureau ◽  
John Weigand
Keyword(s):  
Cervus Elaphus ◽  
Ursus Arctos ◽  
Age Distribution ◽  
Grizzly Bear ◽  
Gray Wolf ◽  
River Drainage ◽  
Felis Concolor ◽  
The North ◽  
North Fork ◽  
Flathead River

During the reporting period, major goals of this project were to monitor elk (Cervus elaphus) in the North Fork of the Flathead River Drainage for mortality, monitor seasonal distribution and determine key areas of use, establish a repeatable index of elk abundance, and determine age/sex composition. Two radio collared elk have died during the last six months. Both elk were killed in May by mountain lions (Felis concolor). This brings the mortality totals to seven elk killed by lions, two by wolves (Canis lupus), one by grizzly bear (Ursus arctos horribilis), and one by a hunter (n=34 radio-collared elk). Lions killed elk throughout the age distribution. Wolves took a calf and an old elk. The hunter killed a prime-aged elk, while the grizzly killed a 16-year-old elk.

Scat detection dogs in wildlife research and management: application to grizzly and black bears in the Yellowhead Ecosystem, Alberta, Canada

2004 ◽  
Vol 82 (3) ◽  
pp. 475-492 ◽  
Author(s):  
Samuel K Wasser ◽  
Barbara Davenport ◽  
Elizabeth R Ramage ◽  
Kathleen E Hunt ◽  
Margaret Parker ◽  
...  
Keyword(s):  
Ursus Arctos ◽  
Physiological Stress ◽  
Black Bear ◽  
Reproductive Activity ◽  
Grizzly Bears ◽  
Grizzly Bear ◽  
Fecal Cortisol ◽  
The North ◽  
Promising Tool ◽  
Northern Portion

We report the development and application of a method using domestic dogs (Canis familiaris Linnaeus, 1758) to systematically locate wildlife scat over large remote areas. Detection dogs are chosen for their strong object orientation, high play drive, and willingness to strive for a reward. Dogs were trained to detect grizzly bear (Ursus arctos Linnaeus, 1758) and black bear (Ursus americanus Pallas, 1780) scats over a 5200-km2 area of the Yellowhead Ecosystem, Alberta, Canada. DNA from scat provided the species and (for grizzly bears only) sex and individual identities of the animal at each location. Concentrations of fecal cortisol and progesterone metabolites from these same grizzly bear scats provided indices of physiological stress and reproductive activity (in females), respectively. Black and grizzly bears were most concentrated in the northern portion of the multiuse study area, where food is most abundant yet poaching-related mortality appears to be heaviest. Physiologic stress was also lowest and female reproductive activity correspondingly highest for grizzly bears in the north. The scat-based distributions corresponded to concurrently collected hair-snag data in 1999 and global positioning system radiotelemetry data (of grizzly bears) in 1999 and 2001. Results suggest that the scat dog detection methodology provides a promising tool for addressing a variety of management and research questions in the wildlife sciences.

Dynamics of a grizzly bear population during a period of industrial resource extraction. II. Mortality rates and causes of death

1989 ◽  
Vol 67 (8) ◽  
pp. 1861-1864 ◽  
Author(s):  
Bruce N. McLellan
Keyword(s):  
Outdoor Recreation ◽  
Ursus Arctos ◽  
Survival Rates ◽  
Timber Harvest ◽  
Easy Access ◽  
Resource Extraction ◽  
Grizzly Bears ◽  
Grizzly Bear ◽  
Human Intervention ◽  
Management Actions

The causes and rates of grizzly bear (Ursus arctos) mortality in a radio-marked population in southeastern British Columbia were studied for 9 years during a period of timber harvest, gas exploration, and outdoor recreation, including grizzly hunting. During 110 bear-years of radio tracking 55 radio-collared grizzly bears and their dependent offspring, one bear with a functioning radio collar died from natural causes and eight others from human intervention; in addition, four dependent offspring were thought to have died. Excluding trap-related mortalities, the best estimate for the annual survival rates were as follows: 0.82 for cubs, 0.88 for yearlings, 0.93 for subadults, and 0.93 for adults. Of the eight bears killed by human intervention, two were killed by legal harvest, five by illegal harvest (one of these in a trap), and one was killed in a trap by another bear. No mortalities were directly attributable to industrial activities. Resource extraction industries do contribute to grizzly bear mortality indirectly through the construction of roads, which provide easy access to hunters, poachers, and settlers. Road access planning and postoperational control of vehicles are recommended management actions.

A grizzly bear from the Middle Wisconsin of Woodbridge, Ontario

1976 ◽  
Vol 13 (2) ◽  
pp. 341-347 ◽  
Author(s):  
Charles S. Churcher ◽  
Alan V. Morgan
Keyword(s):  
Ursus Arctos ◽  
Grizzly Bears ◽  
Grizzly Bear ◽  
Bone Fragment ◽  
Mammuthus Primigenius ◽  
Ursus Arctos Horribilis ◽  
Before And After ◽  
Lake Simcoe ◽  
Left Humerus ◽  
Woolly Mammoth

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.

Spatially explicit carrying capacity estimates to inform species specific recovery objectives: Grizzly bear (Ursus arctos) recovery in the North Cascades

2018 ◽  
Vol 222 ◽  
pp. 21-32 ◽  
Author(s):  
Andrea L. Lyons ◽  
William L. Gaines ◽  
Peter H. Singleton ◽  
Wayne F. Kasworm ◽  
Michael F. Proctor ◽  
...  
Keyword(s):  
Carrying Capacity ◽  
Ursus Arctos ◽  
Spatially Explicit ◽  
Grizzly Bear ◽  
North Cascades ◽  
The North ◽  
Species Specific ◽  
Capacity Estimates

Predation on moose and caribou by radio-collared grizzly bears in east central Alaska

1988 ◽  
Vol 66 (11) ◽  
pp. 2492-2499 ◽  
Author(s):  
R. D. Boertje ◽  
W. C. Gasaway ◽  
D. V. Grangaard ◽  
D. G. Kelleyhouse
Keyword(s):  
Important Implication ◽  
Rangifer Tarandus ◽  
Ursus Arctos ◽  
Prey Availability ◽  
Grizzly Bears ◽  
Grizzly Bear ◽  
East Central ◽  
Specific Factors ◽  
Low Levels ◽  
Predation Rates

Radio-collared grizzly bears (Ursus arctos) were sighted daily for approximately 1-month periods during spring, summer, and fall to estimate predation rates. Predation rates on adult moose (Alces alces) were highest in spring, lowest in summer, and intermediate in fall. The highest kill rates were by male grizzlies killing cow moose during the calving period. We estimated that each adult male grizzly killed 3.3–3.9 adult moose annually, each female without cub(s) killed 0.6–0.8 adult moose and 0.9–1.0 adult caribou (Rangifer tarandus) annually, and each adult bear killed at least 5.4 moose calves annually. Grizzly predation rates on calves and grizzly density were independent of moose density and are probably more related to area-specific factors, e.g., availability of alternative foods. An important implication of our results is that managers should not allow moose densities to decline to low levels, because grizzlies can have a greater relative impact on low- than on high-density moose populations and because grizzly predation can be difficult to reduce. Grizzly bears were primarily predators, rather than scavengers, in this area of low prey availability (11 moose/grizzly bear); bears killed four times more animal biomass than they scavenged.

A study of predominant aerobic microflora of black bears (Ursus americanus) and grizzly bears (Ursus arctos) in northwestern Alberta

1987 ◽  
Vol 33 (11) ◽  
pp. 949-954 ◽  
Author(s):  
L. J. Goatcher ◽  
M. W. Barrett ◽  
R. N. Coleman ◽  
A. W. L. Hawley ◽  
A. A. Qureshi
Keyword(s):  
Soil Bacteria ◽  
Ursus Arctos ◽  
Random Distribution ◽  
Ursus Americanus ◽  
Black Bear ◽  
Black Bears ◽  
Grizzly Bears ◽  
Grizzly Bear ◽  
Streptococcus Species ◽  
Generic Composition

Swab specimens were obtained from nasal, rectal, and preputial or vaginal areas of 37 grizzly and 17 black bears, captured during May to June of 1981 to 1983, to determine the types and frequency of predominant aerobic microflora. Bacterial genera most frequently isolated from bears were Escherichia, Citrobacter, Hafnia, Proteus, Staphylococcus, and Streptococcus species, comprising about 65% of the isolates. Erwinia, Xanthomonas, Agrobacterium, Rhizobium, and Gluconobacter/Acetobacter were also isolated but at lower frequencies (< 5%). Comparison of bacterial generic composition using similarity quotient values showed no appreciable differences between grizzly and black bear flora. Also, no outstanding differences in bacterial generic composition were observed among grizzly bear samples; however, differences were noted among black bear samples. Fungal genera most commonly encountered included Cryptococcus, Rhodotorula, Cladosporium, Penicillium, Sporobolomyces, and Candida. In general, the microflora of both bear types were marked by generic diversity and random distribution. The majority of microorganisms isolated from the plant samples in the study area were also found in bear samples. This observation and the presence of certain water and soil bacteria in samples from bears suggest that the predominant microflora of both grizzly and black bears were transient and probably influenced by their foraging habits and surrounding environments.

Demography of barren-ground grizzly bears

2003 ◽  
Vol 81 (2) ◽  
pp. 294-301 ◽  
Author(s):  
Philip D McLoughlin ◽  
Mitchell K Taylor ◽  
H Dean Cluff ◽  
Robert J Gau ◽  
Robert Mulders ◽  
...  
Keyword(s):  
Survival Rate ◽  
Litter Size ◽  
Birth Interval ◽  
Ursus Arctos ◽  
Survival Rates ◽  
Grizzly Bears ◽  
Adult Males ◽  
Barren Ground ◽  
Rate Of Increase ◽  
The Mean

Between May 1995 and June 1999, we equipped 81 barren-ground grizzly bears (Ursus arctos) with satellite radio collars within a study area of 235 000 km2, centred 400 km northeast of Yellowknife, Northwest Territories, Canada. We used data from radiotelemetry to estimate survival rates, reproductive parameters, and the finite rate of increase of the population (λ). The annual survival rate of adult females was estimated at 0.979 (95% confidence intervals (CI) = 0.955–0.998), while the survival rate of adult males was 0.986 (95% CI = 0.942–1.0). The cub survival rate was 0.737 (95% CI = 0.600–0.844) and the yearling survival rate was 0.683 (95% CI = 0.514–0.821). Cub litter size averaged 2.23 (SE = 0.13, n = 35), while yearling litter size decreased to a mean of 1.86 (SE = 0.12, n = 35). The mean litter size of females with 2-year-olds was 1.85 (SE = 0.15, n = 20). The mean birth interval was 2.8 years (SE = 0.3 years, n = 17). The mean reproductive interval, which is calculated by excluding the loss of whole litters from the sample, was 3.9 years (SE = 0.4 years, n = 9). Mean litter size divided by mean birth interval yielded an annual natality rate of 0.81 cubs per adult female per year. The mean age at first parturition was 8.1 years (SE = 0.5 years, n = 10). We believe the population to be currently stable or slightly increasing (λ = 1.033, 95% CI = 1.008–1.064).

Use of stable isotopes to determine diets of living and extinct bears

1996 ◽  
Vol 74 (11) ◽  
pp. 2080-2088 ◽  
Author(s):  
G. V. Hilderbrand ◽  
S. D. Farley ◽  
C. T. Robbins ◽  
T. A. Hanley ◽  
K. Titus ◽  
...  
Keyword(s):  
Ursus Arctos ◽  
Isotopic Fractionation ◽  
Columbia River ◽  
Late Summer ◽  
Isotopic Signature ◽  
Grizzly Bears ◽  
Brown Bears ◽  
River Drainage ◽  
Carbon And Nitrogen ◽  
Isotopic Analyses

The potential use of stable-isotope analyses (δ13C and δ15N) to estimate bear diets was assessed in 40-day feeding trials using American black bears (Ursus americanus). Bear plasma and red blood cells have half-lives of ~4 days and ~28 days, respectively. The isotopic signature of bear plasma is linearly related to that of the diet, and with the exception of adipose tissue, there is no isotopic fractionation across bear tissues. Isotopic analyses were used to estimate the diets of three bear populations: Pleistocene cave bears (U. speleaus) in Europe, grizzly bears (Ursus arctos horribilis) inhabiting the Columbia River drainage prior to 1931, and brown bears (U. arctos) of Chichagof and Admiralty islands, Alaska. Cave bears were omnivores with terrestrially produced meat contributing from 41 to 78% (58 ± 14%) of their metabolized carbon and nitrogen. Salmon contributed from 33 to 90% (58 ± 23%) of the metabolized carbon and nitrogen in grizzly bears from the Columbia River drainage. Finally, most brown bears on Chichagof and Admiralty islands feed upon salmon during the late summer and fall; however, a subpopulation of bears exists that does not utilize salmon.

scholarly journals The Genome of the North American Brown Bear or Grizzly: Ursus arctos ssp. horribilis

Genes ◽  
2018 ◽  
Vol 9 (12) ◽  
pp. 598 ◽  
Author(s):  
Gregory A. Taylor ◽  
Heather Kirk ◽  
Lauren Coombe ◽  
Shaun D. Jackman ◽  
Justin Chu ◽  
...  
Keyword(s):  
Ursus Arctos ◽  
Brown Bear ◽  
Close Relative ◽  
Grizzly Bear ◽  
Construction Technique ◽  
Protein Coding ◽  
Automated Annotation ◽  
The North ◽  
Long Read ◽  
Reference Quality

The grizzly bear (Ursus arctos ssp. horribilis) represents the largest population of brown bears in North America. Its genome was sequenced using a microfluidic partitioning library construction technique, and these data were supplemented with sequencing from a nanopore-based long read platform. The final assembly was 2.33 Gb with a scaffold N50 of 36.7 Mb, and the genome is of comparable size to that of its close relative the polar bear (2.30 Gb). An analysis using 4104 highly conserved mammalian genes indicated that 96.1% were found to be complete within the assembly. An automated annotation of the genome identified 19,848 protein coding genes. Our study shows that the combination of the two sequencing modalities that we used is sufficient for the construction of highly contiguous reference quality mammalian genomes. The assembled genome sequence and the supporting raw sequence reads are available from the NCBI (National Center for Biotechnology Information) under the bioproject identifier PRJNA493656, and the assembly described in this paper is version QXTK01000000.

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