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

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.

1989 ◽  
Vol 67 (8) ◽  
pp. 1856-1860 ◽  
Author(s):  
Bruce N. McLellan

The characteristics of a grizzly bear (Ursus arctos) population in southeastern British Columbia were studied between 1979 and 1986, a period of timber harvest, gas exploration, and outdoor recreation, including grizzly hunting. I investigated the hypothesis that collectively these activities were detrimental to the grizzly population. I predicted a low density of bears compared with other interior populations and (or) a negative rate of increase. The sex ratio of cubs and yearlings captured was 50:50 and they represented 21.5 and 17.5% of the population, respectively. Although more adult males than adult females were captured, I estimated that there were more adult females than males in the population. I used two methods of population estimation and assumed saturation trapping : one method was based on home range characteristics and the other on the proportion of aerial locations in the study area. The average estimated bear density was 6.4/100 km2, which was high for an interior population, and increased from approximately 5.7/100 km2 in 1981 to 8.0/100 km2 in 1986, for an average annual observed rate of increase of r = 0.07.


1989 ◽  
Vol 67 (8) ◽  
pp. 1865-1868 ◽  
Author(s):  
Bruce N. McLellan

Reproductive parameters and rate of increase were estimated for a grizzly bear (Ursus arctos) population in southeastern British Columbia during a period of timber harvest and gas exploration, 1979–1987.I hypothesized that these activities would be detrimental to the population and predicted a negative rate of increase. There was an average of 2.26 cubs in 31 litters. The average of nine interbirth intervals was 2.67 years, and the average age at which five females produced their first litter was 6 years. The population's annual reproductive rate calculated by three methods averaged 0.86 cubs per adult female. By iteration of the Lotka equation, the best estimate of the exponential rate of increase was 0.081. Industrial activities did not appear to have a significant detrimental effect on the grizzly bear population in the Flathead Valley during the period of study but the roads built provided easy access for hunters and poachers.


1996 ◽  
Vol 74 (8) ◽  
pp. 1409-1416 ◽  
Author(s):  
Frederick W. Hovey ◽  
Bruce N. McLellan

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.


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.


1988 ◽  
Vol 66 (11) ◽  
pp. 2492-2499 ◽  
Author(s):  
R. D. Boertje ◽  
W. C. Gasaway ◽  
D. V. Grangaard ◽  
D. G. Kelleyhouse

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.


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

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.


2003 ◽  
Vol 81 (2) ◽  
pp. 294-301 ◽  
Author(s):  
Philip D McLoughlin ◽  
Mitchell K Taylor ◽  
H Dean Cluff ◽  
Robert J Gau ◽  
Robert Mulders ◽  
...  

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).


1984 ◽  
Vol 62 (12) ◽  
pp. 2571-2575 ◽  
Author(s):  
Anne C. Holcroft ◽  
Stephen Herrero

Characteristics of sites where Hedysarum sulphurescens Rydb. roots were extensively, less extensively, or not dug by grizzly bears Ursus arctos horribilis Ord. were analyzed in relation to topographic, vegetative, soil, and geologic features. Discriminant function analysis significantly separated dug and undug sites, but did not separate extensively and less extensively dug sites. Ease of breaking the soil surface, presence of shaly rock fragments, loose cobble and gravel, and steep slopes were characteristic of dug sites. The abundance of H. sulphurescens appeared less important than the loose nature of the substrate indicating that digging time was important in optimizing energetics.


PeerJ ◽  
2018 ◽  
Vol 6 ◽  
pp. e5781
Author(s):  
Bruce N. McLellan ◽  
Garth Mowat ◽  
Clayton T. Lamb

Managing the number of grizzly bear (Ursus arctos) mortalities to a sustainable level is fundamental to bear conservation. All known grizzly bear deaths are recorded by management agencies but the number of human-caused grizzly bear deaths that are not recorded is generally unknown, causing considerable uncertainty in the total number of mortalities. Here, we compare the number of bears killed legally by hunters to the number killed by people for all other reasons, for bears wearing functioning radiocollars and for uncollared bears recorded in the British Columbia (BC) government mortality database for the Flathead Valley in southeast BC. Between 1980 and 2016, permitted hunters killed 10 collared bears and 12 (9 known, 3 suspected) were killed by people for other reasons. This ratio differed (p < 0.0001) from the uncollared bears in the government database where 71 were killed by hunters while only 10 were killed for other reasons. We estimate that 88% (95% CI; 67–96%) of the human-caused mortalities that were not by permitted hunters were unreported. The study area may have low reporting rates because it is >40 km on a gravel road from a Conservation Officer office, so reporting is difficult and there are no human residences so there is little concern of a neighbor contacting an officer. Our results are likely indicative of other places that are road-accessed but far from settlements. We discuss the implications of sampling individuals for collaring and the possible implications of wearing a collar on the animal’s fate.


Rangifer ◽  
2000 ◽  
Vol 20 (5) ◽  
pp. 17 ◽  
Author(s):  
Rodney D. Boertje ◽  
Craig L. Gardner

A diverse, international Fortymile Planning Team wrote a novel Fortymile caribou herd {Rangifer tarandus granti) Management Plan in 1995 (Boertje &amp; Gardner, 1996: 56-77). The primary goal of this plan is to begin restoring the Fortymile herd to its former range; &gt;70% of the herd's former range was abandoned as herd size declined. Specific objectives call for increasing the Fortymile herd by at least 5-10% annually from 1998-2002. We describe demographics of the herd, factors limiting the herd, and condition of the herd and range during 1992-1997. These data were useful in proposing management actions for the herd and should be instrumental in future evaluations of the plan's actions. The following points summarize herd biology relevant to management proposed by the Fortymile Planning Team: 1. Herd numbers remained relatively stable during 1990-1995 (about 22 000-23 000 caribou). On 21 June 1996 we counted about 900 additional caribou in the herd, probably a result of increased pregnancy rates in 1996. On 26 June 1997 we counted about 2500 additional caribou in the herd, probably a result of recruitment of the abundant 1996 calves and excellent early survival of the 1997 calves. The Team deemed that implementing management actions during a period of natural growth would be opportune. 2. Wolf (Canis lupus) and grizzly bear (Ursus arctos) predation were the most important sources of mortality, despite over a decade of the most liberal regulations in the state for harvesting of wolves and grizzly bears. Wolves were the most important predator. Wolves killed between 2000 and 3000 caribou calves annually during this study and between 1000 and 2300 older caribou; 1200-1900 calves were killed from May through September. No significant differences in annual wolf predation rates on calves or adults were observed between 1994 and early winter 1997. Reducing wolf predation was judged by the Team to be the most manageable way to help hasten or stimulate significant herd growth. To reduce wolf predation, the Team envisioned state-sponsored wolf translocations and fertility control in 15 key wolf packs during November 1997-May 2001. Also, wolf trappers were encouraged to shift their efforts to specific areas. 3. To increase social acceptance of the management plan, the Fortymile Team proposed reducing the annual caribou harvest to 150 bulls for 5 years beginning in 1996. Reducing annual harvests from 200-500 bulls (&lt;2% of the herd, 1990-1995) to 150 bulls (&lt;1% of the herd, 1996-2000) will not result in the desired 5-10% annual rates of herd increase. 4. We found consistent evidence for moderate to high nutritional status in the Fortymile herd when indices were compared with other Alaskan herds (Whitten et al, 1992; Valkenburg, 1997). The single evidence for malnutrition during 1992-1997 was the low pregnancy rate during 1993 following the abnormally short growing season of 1992. However, this low pregnancy rate resulted in no strong decline in Fortymile herd numbers, as occurred in the Delta and Denali herds (Boertje et al, 1996). No significant diseases were found among Fortymile caribou. 5. Winter range can support elevated caribou numbers both in regards to lichen availability on currently used winter range and the availability of vast expanses of winter range formerly used by the herd.


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