Gibeau, Michael. 1998. Grizzly bear habitat
effectiveness model for Banff, Yoho and Kootenay National Parks. Ursus
10:235-241.
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GRIZZLY BEAR HABITAT
EFFECTIVENESS MODEL FOR BANFF, YOHO, AND KOOTENAY NATIONAL PARKS, CANADA
Michael L. Gibeau
Abstract: Changes in land use are currently accelerating
development pressures in the Central Canadian Rocky Mountains. Given the
existing and proposed human influences in the region, cumulative effects
are a major issue, especially for carnivores. I quantitatively and
qualitatively assess of the effects of human actions on grizzly bears (Ursus
arctos horribilis) and their habitat. Since 1985, a cumulative effects
model (CEM) for grizzly bears has evolved into the consolidated form used
by the US Department of Agriculture (USDA) Forest Service. The habitat
effectiveness model presented in this paper follows the USDA Forest
Service CEM with minor changes to allow our data to conform to the
process. I analyzed a study area of approximately 9,300 km2,
and results indicate that much of the 3 National Parks are only moderately
productive habitat, excluding human influences. Adding the effects of
humans, the modelled ability of the landscape to support bears is
significantly reduced. The model suggests widespread habitat alienation in
what is supposed to be core refugia for grizzly bears, questioning the
ability of the landscape to support a viable population. This situation we
find ourselves in is a particularly difficult one, given that incremental
recreational development has never been considered a threat to the
protected status of Canadian national parks. In the Canadian Rockies,
mountain national parks function as de facto core refugia for
grizzly bears. With continued erosion of grizzly bear habitat in what is
supposed to be core refugia, time is clearly not on the park manager's
side. Swift, and in some cases, drastic, management action is needed if we
are to stem grizzly bear extinction within the ecosystem.
Ursus 10:235-241
Key words: Canada, grizzly bear, habitat, model, national parks, Ursus
arctos horribilis
As demands on the land increase, cumulative effects result from
individually minor yet collectively significant uses occurring over space
and time. Cumulative effects analysis (CEA) assess the effects on a system
of spatial and temporal perturbations resulting from human activities (Beanlands
et al. 1986). This is a fundamental paradigm shift for wildlife
conservation, as we can no longer wait for scientific proof of simple
cause and effect relationships (Davies 1992). CEA explicitly deals with
effects, and most importantly, whether those effects exceed or fall short
of thresholds compatible with population goals of a given species or guild
of species. Hence, CEA and its subsequent models are tools to perform
proactive conservation (Weaver et al. 1987) of threatened or sensitive
species and landscapes.
Changes in land use are currently accelerating development in the
Central Canadian Rocky Mountains. Unparalleled development has occurred in
the mountain national parks since 1980 including hotels, ski areas,
campgrounds, golf courses, backcountry lodges, and an extensive network of
equestrian, hiking, and ski trails. Two major transcontinental
transportation routes, the Trans Canada Highway and the CP Rail mainline,
bisect Banff and Yoho National Parks. This area can be described as one of
the most intensively developed landscapes in the world where grizzly bears
still survive (S. Herrero, Univ. of Calgary, AB, Canada, pers. commun.,
1995). The result is a loss of connectivity as well as potential loss of
viability for carnivore metapopulations. Given existing and proposed human
activities in the Central Rockies area, cumulative deleterious effects are
affecting wildlife, especially carnivores. CEA is becoming a recognized
legal and policy approach to environmental impact assessment (Spaling and
Smit 1993). Parks Canada recognizes that proactive measures are necessary
now to ensure long-term viability of carnivore metapopulations (Apps
1993).
A CEA for grizzly bears has several components (Mattson and Knight
1991), including: (1) detailed habitat description and capability
analysis; (2) comprehensive accounting of all current and proposed human
activities and developments; (3) establishment of population threshold
levels; and (4) population viability analysis. CEA must be done on some
meaningful spatial and temporal scale (Comm. Appl. Ecol. Theory to
Environ. Problems 1986) and must include the entire population to
meaningfully assess human impacts with respect to the population's chances
for survival (Shaffer and Sampson 1985, Gilpin 1987, Grumbine 1990).
Herein I discuss the application of a tool developed to quantitatively
and qualitatively assess the effects of human actions on grizzly bears and
their habitat. Since 1985, a cumulative effects model (CEM) for grizzly
bears has evolved into the consolidated form presented by the US
Department of Agriculture (USDA) Forest Service (1990). The model includes
the past and present human impacts on grizzly bears and their habitat. The
habitat effectiveness model I present follows the USDA Forest Service CEM
with minor changes to allow our data to conform with the process. This
model is an analytical aid to decisions affecting conservation of grizzly
bears in the Rocky Mountains.
I acknowledge D. Mattson, T. Puchlerz, and R. Rankin for their
assistance in the application of a complex model. G. Moir and J. Slemko
provided computer technical support. Special thanks to J. Weaver for his
insights and guidance through the process.
STUDY AREA
Banff, Yoho, and Kootenay National Parks form a contiguous area of
approximately 9,300 km2 along the continental ranges of the
Central Canadian Rocky Mountains (Fig. 1). Topographic features include
rugged mountain slopes, steep-sided ravines, and flat valley bottoms. The
climate is continental with long, cold winters and short, cool summers.
The aspect and elevation of the mountainous topography modifies climate
somewhat. Topography, soil, and local climate strongly influence
vegetative communities. Vegetation can be classified into major ecoregions:
montane (1,300 to 1,600 m), subalpine (1,600 to 2,300 m) and alpine
(2,300+ m). The montane region is dominated by dry grasslands, wet
shrubland, and forests of Lodgepole pine (Pinus contorta),
Douglas-fir (Pseudotsuga menziesii), white spruce (Picea glauca)
and aspen (Populus tremuloides). Subalpine areas are forested with
mature stands of lodgepole pine, Engelman spruce (Picea engelmanii),
subalpine fir (Abies lasiocarpa), and subalpine larch (Larix
lyallii) interspersed by areas of wetland shrub. A mosaic of low
shrubs and herbs characterize alpine areas.
METHODS
Several types of data were required to produce a habitat effectiveness
model; each data set had inherent assumptions and errors. All analyses
were based on 1:50,000 scale mapping; therefore, data are probably not
sufficiently accurate for evaluating mitigation scenarios on an
activity-by-activity basis. Data compilation and analysis were facilitated
by Spans® GIS (Intera Tydac Technologies Inc) and Quattro Pro® (Borland
International Inc) spreadsheet program.
The study area was subjectively divided into bear management units (BMU)
based on topographic features, human facilities, and areas of known high
bear use. This division of the landscape was done to: (1) assess existing
and proposed activities without having effects diluted by a large area;
(2) correlate grizzly bear use to habitat ecology; (3) identify contiguous
complexes of habitat which meet year-long needs of grizzly bears; and (4)
prioritize areas where management needs require closer scrutiny (USDA For.
Serv. 1990).
Habitat Component
Grizzly bear habitat data were taken directly from a habitat evaluation
of the 4 mountain parks by Kansas and Riddell (1995). This study applied a
food habits model to the Ecological Land Classifications (ELC) of the
Western Region of Parks Canada. For their model, Kansas and Riddell (1995)
identified key bear foods through food habits and habitat-use data from
previous studies (Russell et al. 1979, Hamer and Herrero 1983, Hamer et
al. 1985, Raine and Riddell 1991). They assigned a value from 0 to 10 for
ELC polygons in each park to reflect their importance for grizzly bears
for each month. To reduce the volume of data, similar ELC polygons were
grouped into "functional units" and also assigned a value from 0
to 10 for each month.
I used functional unit values to evaluate potential habitat for each
BMU each month following the USDA Forest Service (1990) CEM habitat
routine. Months were grouped into spring (April, May, and June), summer
(July and August), and fall (September and October) after calculations
were complete. Readers should refer to the USDA Forest Service (1990) CEM
for these computational formulas.
The output from this routine is the habitat component for the
effectiveness model. In essence, our habitat component is a qualitative
assessment of the spatial and temporal distribution of grizzly bear foods
for the 3 parks. The habitat evaluation generated a table of values from 0
to 10, rating potential grizzly bear habitat in each BMU based on
spatial and temporal distribution of foods for each season. A BMU rated 0
is interpreted as of no value to grizzly bears, whereas a BMU rated 10
translates to the best possible habitat available in a given season.
Disturbance Component
The disturbance component for the effectiveness model uses human
activity maps from previous ecosystem studies (Komex International 1995).
These maps use vector, point, and polygon data categorized into 7 classes
on an exponential scale based on park visitation records and personal
observation. These data became the basis for delineation of the types and
intensity of human uses and their associated disturbance values. The major
assumption of the human activity model is that it accurately reflects
human use at an ecosystem scale. Underlying assumptions of the disturbance
component are listed in the USDA Forest Service (1990) CEM.
Following the USDA Forest Service (1990) CEM, our human use model was
stratified based on: (1) motorized or nonmotorized type of activity; (2)
point or linear nature of activity; (3)high or low intensity of activity;
and (4) cover or noncover security class. Linear activity included
highways and trails. Point activity included campgrounds, lodges, and
other developments. High use was defined as >100 vehicles or
people/month, low use was defined as <100 vehicles or people/month. The
USDA Forest Service model used 80 vehicles or parties/month as the
division between high and low use. Based on the ELC, cover was defined as
forested ecosites and noncover, grassland and alpine ecosites.
Once stratified, each activity group was assigned a disturbance
coefficient and associated zone of influence. The zone of influence
(measured horizontally) identified the area in which grizzlies would be
affected by the activity; the coefficient identified the degree of
disturbance within the zone of influence. The degree of habituation of a
bear population and the type of human activities (recreation, resource
extraction, or hunting) influences bear behaviour. The consequences of
bears habituating to or avoiding people were incorporated into disturbance
coefficients and associated zones of influence. Disturbance can influence
bear use through actual displacement and change in use patterns reducing
the time available for a bear to use an area (e.g., 24 hour to nocturnal
only use). These factors were considered in coefficient development.
Disturbance coefficients are rated on a scale of 0 to 1 based on how
grizzly bears would respond to a given activity (e.g., what percent of the
bears would still use the habitat within the zone of influence for what
percent of a 24-hour period). For example, a disturbance coefficient of 0
implies total displacement - none of the habitat within the zone of
influence would be available to the bear. A disturbance coefficient of 1
indicates no disturbance - the accessability to the habitat within the
zone of influence is not affected by the activity. A disturbance
coefficient of 0.5 indicates that an area's ability to support bears is 50
% of potential. Either half of the bears have been displaced or all the
bears can use the area only half of the time, or any combination. The
result is the same: the ability to support bears is reduced by 50 %.
For this model, disturbance coefficients and zones of influence from
the Yellowstone ecosystem (May 1993) were adopted for the types and
intensities of human use (Table 1). Coefficients from the Yellowstone
ecosystem were chosen because (1) there is no empirical data on human
influences in the Canadian Rocky Mountains; (2) this study area has
similar types of human influences on grizzly bears given a protected core
surrounded by multiple-use lands; and (3) more research has been done on
human effects in the Yellowstone ecosystem than other areas. Consultation
with knowledgeable individuals (D. Mattson, Univ. of Idaho, Moscow, 1994;
T. Puchlerz, USDA For. Serv., Missoula, MT, 1994; pers. commun.) concurred
the Yellowstone situation is analogous to the 3 Canadian mountain parks.
Some minor modifications to Yellowstone's security cover classes were
necessary to allow our data to fit the model. Yellowstone's model
incorporates 5 security classes whereas, this model only incorporates 2.
I multiplied disturbance coefficients by the habitat value within that
affected portion of a polygon to compute disturbance values. Disturbance
within overlapping zones of influence were cumulative, hence coefficients
were multiplied together. Again, readers should refer to the USDA Forest
Service(1990) CEM for detailed methodology and formulas.
The disturbance component generated a table of numeric values from 0 to
10 rating the realized ability of grizzly bears to continue using
habitats influenced by human activity. The same units of measurement are
used as the habitat component allowing comparisons between inherent
habitat quality and altered conditions. A BMU rated 0 is interpreted as of
no value to grizzly bears, whereas a rating of 10 translates to the best
possible habitat left. The disturbance component illustrates alienation
within BMU unit by season. Output from this routine measures the ability
of bears to continue using habitat influenced by human activity.
Habitat Effectiveness
Habitat effectiveness is the comparison of the habitat and disturbance
components and reflects an area's actual ability to support bears.
Comparison of the habitat and disturbance components produces a table of
habitat effectiveness values for each BMU that represent the percentage of
potential for that area by season. These numeric values are interpreted
simply as what percentage is left after accounting for human disturbances
imposed upon the area.
Interpretation of habitat effectiveness as a percent of pristine cannot
be translated into number of bears lost. The CEM process is still under
development, and the information needed to state actual effects on the
grizzly bear population (numbers of bears) is not known. Therefore, it
oversteps the bounds of the model to attempt to determine the number of
bears that could be supported by restoring an area to natural conditions.
Likewise, population losses resulting from further development cannot be
determined. The numbers generated by the model are for comparison of
alternatives only.
RESULTS
The habitat component provides a measure of the inherent potential or
productivity of the landscape for spring, summer, and fall. Values range
from very high capability such as BMU 40 (8.0 spring, 8.1 summer, 8.4
fall) to low capability such as BMU 1 (1.9 spring, 1.5 summer, 1.7 fall).
Habitat component results for summer were categorized into very high
(>7), high (5.0 to 6.9), moderate (3.0 to 4.9) and low (<2.9)
potential (Fig. 2). Values for spring and fall were similar to summer
values (Table 2).
The disturbance component is used to compare and contrast habitat
productivity when human influences are considered. Model output depicts
dramatic declines from potential in some BMUs. For example, in Banff
National Park 18% of the BMUs were inherently low potential in summer.
However, when human disturbance was added, 48% of the BMUs in Banff
National Park had low realized productivity. Disturbance components for
summer were categorized into very high (>7), high (5.0 to 6.9),
moderate (3.0 to 4.9) and low (<2.9) realized grizzly bear habitat
(Fig. 3). Values for spring and fall were similar to summer values (Table
2).
The habitat effectiveness value quantifies the extent of landscape
available to bears when human influences are considered. Figure 4 displays
habitat effectiveness for summer categorized into 4 percentages of
potential. For many BMUs the model suggests that the ability of the
landscape to support bears has been significantly reduced. For example,
BMU 19 is 78.6% of potential in the summer (Table 2). In other words, it
is 21.4% disturbed.
To summarize the analysis and give perspective on the entire landscape,
all 40 BMUs can be combined. In total, my analysis covered 9,344 km2 of de facto core refugia within the Central Canadian Rockies. Using
summer values, the area has a modelled potential habitat value of 4.4, a
realized habitat value of 3.6 and a habitat effectiveness value of 83.1%.
DISCUSSION
It becomes obvious that a significant portion of the landscape is only
moderately productive habitat (Fig. 2). Much of this is due to
unproductive land within individual BMUs. For example, BMU 1 is 70% rock
and ice. Much of the mountain national parks are not inherently prime
grizzly habitat; this is a new concept for many and an important
realization in understanding the basis for CEA. National parks in the
Canadian Rocky Mountains were originally selected for their scenic and
tourism value, which is inherently not good habitat. Better habitat lies
to both the east and west in human-dominated multiple-use lands. Yet the
disturbance component suggested wide spread habitat alienation in areas
considered core refugia for grizzly bears in the Canadian Rocky Mountains.
This questions the ability of the landscape as a whole to support a viable
population.
There has been considerable discourse regarding habitat threshold
levels beyond which grizzly bears are eliminated. In the U.S., researchers
have been working toward establishing meaningful ecological thresholds,
but how to do this remains unclear. One way of establishing thresholds is
to view them as some acceptable percentage of being wrong (D. Mattson,
Univ. of Idaho, Moscow, 1994, pers. commun. ). In the case of the grizzly
bear in the U.S. and Canada, the implications of being wrong have serious
consequences: extinction. If the threshold were set at 80% habitat
effectiveness, would a manager be comfortable with a 20% chance of being
wrong?
In the absence of clearly defined ecological thresholds, I suggest we
add a sociological component to our view of thresholds. What percentage of
human induced degradation are we willing to accept within core refugia or
areas managed as preserves. How degraded can wilderness areas be and still
be called wilderness? These are tough questions with no simple answers. In
the U.S. early CEM models suggested a 70% threshold in the multiple-use
landscape of the Kootenai National Forest. In Yellowstone National Park,
80% has been suggested as a threshold level. If we were to use 80% habitat
effectiveness as the benchmark, 44% of the BMUs in Banff National Park are
close to threshold (Fig. 4).
There are however, still some bears residing in BMUs that are below the
suggested threshold. This can be explained in some cases by the behavioral
concept of persistence of individuals. In long-lived species such as
grizzly bears, individuals will persist and accept the disturbance despite
non-viability because it is home. Once the individual passes on, a new
bear will reject the area due to high levels of human disturbance.
This habitat effectiveness model aggregates the past and present human
effects on grizzly bears and their habitat but does not project into the
future. The model quantifies concerns about the viability of the bear
population within the area of analysis, but it does not confirm them.
Results from long-term empirical work initiated in 1994 test the model and
provide further evidence to justify concern. However, because of time
constraints conservation biologists must be willing to express an opinion
based on available evidence, accepted theory, comparable examples, and
informed judgement (Primack 1993).
A reasonable prediction stemming from the model is that if management
practices do not change, we will continue to erode grizzly bear habitat
and, if unabated, the population will become extinct. To that end, an
independent external review panel was established in 1995 to evaluate
current management practices in Banff National Park and make
recommendations for change.
CONCLUSION
A number of related factors make this situation particularly difficult.
First, much of the mountain national parks are not inherently prime
grizzly habitat, which is a new concept for many. Secondly, the model
suggests the ability of the landscape to support bears has been
significantly reduced by widespread human presence. Finally, traditional
types and levels of human activities are widely accepted within national
parks and have not been viewed as detrimental to grizzly bears.
The status of national parks as protected areas, and therefore refugia
for large carnivores, has been taken for granted since their creation
>100 years ago. Incremental recreational development has never been
considered a threat to this protected status. As we approach the close of
the twentieth century we need to reconsider this paradigm. With continued
erosion of grizzly bear habitat in what is supposed to be core refugia
hanging in the balance, time is clearly not on the park manager's side.
Swift, and in some cases drastic, management action is needed if we are to
stem the progression of extinction within the ecosystem.
LITERATURE CITED
Apps, C. 1993. Cumulative effects assessment for large carnivores: A
literature review and development strategy for the Canadian Rockies. Can.
Parks Serv. Rep., Calgary, AB., 68pp.
Beanlands, G.E., W.J. Erckmann, G.H. Orians, J. O'Riordan, D.
Policansky, M.H. Sadar, and B. Sadler, editors. 1986. Cumulative
environmental effects: a binational perspective. Can. Environ. Assessment
Research Counc., Ottawa, ON, and Natl. Research. Counc, Washington, DC.
175pp.
Committee on the Application of Ecological Theory to Environmental
Problems. 1986. The special problem of cumulative effects. Pages 93-134 in Ecological knowledge and environmental problem-solving. Natl. Acad.
Press, Washington, DC. 388pp.
Davies, K. 1992. An advisory guide on addressing cumulative
environmental effects under the Canadian Environmental Act: a discussion
paper. Fed. Environ. Assessment Rev. Off., Hull, PQ. 43pp.
Gilpin, M.E. 1987. Spatial structure and population vulnerability.
Pages 125-139 in M.E. Soule, ed. Viable populations for
conservation. Cambridge Univ. Press, New York, N.Y.
Grumbine, R.E. 1990. Viable populations, reserve size, and federal land
management: a critique. Conserv. Biol. 4:127-134.
Hamer, D., and S. Herrero, editors. 1983. Ecological studies of the
grizzly bear in Banff National Park. Rep. prep. for Parks Canada by Univ.
Calgary, AB. 303pp.
Hamer, D., S. Herrero, and K. Brady. 1985. Studies of the grizzly bear
in Waterton Lakes National Park. Rep. prep. for Parks Canada by Univ.
Calgary, AB. 163pp.
Kansas, J.L., and R.N. Riddell. 1995. Grizzly bear habitat model for
the 4 contiguous mountain parks, 2nd iteration. Can. Parks Serv. Rep.,
Calgary, AB. 95pp.
Komex International. 1995. Atlas of the Central Rockies Ecosystem. Rep.
to the Central Rockies Interagency Liaison Group. Calgary, AB. 49pp.
Mattson, D.J., and R.R. Knight. 1991. Application of cumulative effects
to the Yellowstone Grizzly Bear Population. U.S. Dept. Inter. Natl. Park
Serv. Interagency Grizzly Bear Study Team Rep. 1991.
Primack, R.B. 1993. Essentials of conservation biology. Sinauer Assoc.
Inc. Sunderland, MA. 564pp.
Raine, R.M., and R.N. Riddell. 1991. Grizzly bear research in Yoho and
Kootenay National Parks. Can. Parks Serv. Rep. Calgary, AB.
Russell, R.H., J. Nolan, N.G. Woody, and G.H. Anderson. 1979. A study
of the grizzly bear (Ursus arctos L.) in Jasper National
Park, 1975-1978. Can. Wildl. Serv., Edmonton, AB. 136pp.
Shaffer, M.L., and F.B.Sampson. 1985. Population size and extinction: a
note on determining critical population sizes. Am. Nat. 125(1):144-152.
Spaling, H., and B. Smit. 1993. Cumulative environmental change:
Conceptual frameworks, evaluation approaches, and institutional
perspectives. Environ. Manage. 17:587-600.
U.S. Department of Agriculture Forest Service. 1990. CEM - A model for
assessing effects on grizzly bears. U.S. Dep. Agric. For. Serv., Missoula,
MT. 24pp.
Weaver, J.L., R.E. Escano, and D.S. Winn. 1987. A framework for
assessing cumulative effects on grizzly bears. North Am. Wildl. and Nat.
Resour. Conf. 52:364-376.
Table 1. Disturbance coefficients and zones of influence for Banff,
Yoho, and Kootenay National Parks habitat effectiveness model, 1995.
Type of activity |
Zone ofinfluence (meters) |
Intensity of use |
Security class |
Coefficient |
Linear motorized |
800 |
High |
Cover |
0.37 |
|
|
|
Non-cover |
0.16 |
|
|
Low |
Cover |
0.73 |
|
|
|
Non-cover |
0.64 |
|
|
|
|
|
Point motorized |
800 |
High |
Cover |
0.37 |
|
|
|
Non-cover |
0.16 |
|
|
Low |
Cover |
0.73 |
|
|
|
Non-cover |
0.64 |
|
|
|
|
|
Linear non-motorized |
400 |
High |
Cover |
0.65 |
|
|
|
Non-cover |
0.56 |
|
|
Low |
Cover |
0.88 |
|
|
|
Non-cover |
0.83 |
|
|
|
|
|
Point non-motorized |
400 |
High |
Cover |
0.50 |
|
|
|
Non-cover |
0.33 |
|
|
Low |
Cover |
0.88 |
|
|
|
Non-cover |
0.83 |
Table 2. Summer values for bear management units (BMUs) in Banff, Yoho,
and Kootenay National Parks habitat effectiveness model, 1995.
BMU |
Potential |
Realized |
Habitat effectiveness |
1 |
1.5 |
1.0 |
66.6 |
2 |
3.1 |
2.7 |
87.1 |
3 |
3.4 |
2.9 |
85.3 |
4 |
2.4 |
2.3 |
95.8 |
5 |
3.0 |
2.2 |
73.3 |
6 |
2.3 |
2.2 |
95.6 |
7 |
2.6 |
2.5 |
96.1 |
8 |
3.5 |
2.6 |
74.3 |
9 |
4.5 |
2.1 |
46.6 |
10 |
3.5 |
3.1 |
88.6 |
11 |
3.2 |
2.5 |
78.1 |
12 |
2.6 |
2.5 |
96.1 |
13 |
4.0 |
3.8 |
95.0 |
14 |
4.1 |
3.8 |
92.7 |
15 |
4.4 |
3.8 |
86.4 |
16 |
5.5 |
3.8 |
69.1 |
17 |
5.2 |
3.9 |
75.0 |
18 |
5.3 |
4.0 |
75.5 |
19 |
5.6 |
4.4 |
78.6 |
20 |
4.8 |
4.7 |
97.9 |
21 |
5.3 |
4.8 |
90.6 |
22 |
7.4 |
3.6 |
48.6 |
23 |
3.5 |
2.9 |
82.8 |
24 |
4.0 |
3.5 |
87.5 |
25 |
5.1 |
4.7 |
92.1 |
26 |
3.5 |
2.9 |
82.8 |
27 |
3.9 |
3.5 |
89.7 |
28 |
4.7 |
4.1 |
87.2 |
29 |
4.4 |
4.1 |
93.2 |
30 |
3.0 |
2.0 |
66.6 |
31 |
4.8 |
3.9 |
81.2 |
32 |
3.6 |
2.8 |
77.7 |
33 |
4.3 |
4.2 |
97.7 |
34 |
4.3 |
3.6 |
83.7 |
35 |
4.8 |
3.9 |
81.2 |
36 |
5.6 |
5.0 |
89.3 |
37 |
6.9 |
6.1 |
88.4 |
38 |
7.8 |
6.7 |
85.9 |
39 |
6.9 |
5.6 |
81.1 |
40 |
8.1 |
6.9 |
85.2 |
Figures not included
Fig. 1 Central Canadian Rocky Mountains. Banff, Yoho, and Kootenay
National Parks are shaded.
Fig. 2 Potential grizzly bear habitat for bear management units in
Banff, Yoho, and Kootenay National Parks, 1995.
Fig. 3 Realized grizzly bear habitat for bear management units in
Banff, Yoho, and Kootenay National Parks, 1995.
Fig. 4 Grizzly bear habitat effectiveness for bear management units in
Banff, Yoho, and Kootenay National Parks, 1995.
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