s 599.7 4446 " (- 1987 I \r ■is *ft.V #» J FlEASE RETUt EAST FRONT GRIZZLY STUDIES STATE DOCUMENTS COLLEGTIOM JAN 2 2 i3&s MONTA!-:.\ STATE LIBRAW. 1515 E. 6th AVE. "HELENA, MONTANA 59620 •% i' '-''^Ifl' \ Prepared by Keith Aune Bob Brannon March, 19S7 JBN 1 0 iSSO MAR2 7W1 JAN 1 5 1993 Mr H an 'JAN 1 4 2004 . •'■ % i . V-" .^■t^ 'iV*«L-W=*!E'S'lll^ :* Mf ! ■ s .I--)*'; f »^./;»f!' ■■ 'M'-^ '■:?Kt '' ' ^ fi '^Z"! i • _!-»4 i sn;iky . ' ^ ■■'■• . ' yl , I *4ri;:-f ' ■ ': ' = '- .-.i- -." '?-l •;•!.!" . *> fj S- ' r^^w "i-f-',^ I' - ' «./, , " -^ © ■ . ' 'S*'r>4 • ■ ; /'':. f-.-- .^, "1 ;•«(■• n' ■• ■ \' ' 'i/" *i ''-^'■hu 'V^-^'v % 1 -■V*' » '.ft* ; fc" '*' ''., , , •i -, «i " Vt - '^- ■ '\n-f ' J -^ ■ "' '^' ' ■ *^ / -•3>.- ,-,''%•'" '^ *'; •;•»,' '. -I fi^ '• I ' ' * , ' rf ■ .■*'<' -. ' iv ' (li, • i- '• - !»• ■-■:'- ■ ~ . '•! , i-fr : *t , ' . . '^ : f-'-l-' 4. ^' *:=>:. '" .. . i£V.* tir .;•• .: ■ t. ^ - _ ' ' . -'i - ■^ ■ •»#_ s ' "' , ' f 1« '^ . .1 " . ■; -;. 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Distribution of 3,170 grizzly bear observations, 1976-86, north of the Sun River. -18- Table 5. The number of observations plotted on the Sun River North- overall and seasonal distribution maps, 1976 - 1986. Period ,, Spring Summer Fall Total 1976-79-' 148 345 205 698 1980 50 83 62 195 1981 186 128 89 403 1982 173 200 148 521 1983 183 189 165 537 1984 84 149 94 327 1985 116 87 71 274 1986 61 92 64 217 TOTAL 1,001 1,273 898 3,172 1 - North of Township 21-22 line. 2 - Reported in Schallenberger and Jonkel, 1980. Figures 5, 6, and 7 show the seasonal distribution of observation data. Seasons are defined as spring (March - June 30) , summer (July 1 - August 30) , and fall (September 1 - November) . Distribution of grizzly bears south of the Sun River was determined by plotting 759 observations gathered between 1976 and 1986 (Fig. 8). A total of 289 observations were reported in Schallenberger and Jonkel (1980) and 470 observations were collected during 1980-86 field seasons. Approximately 40.2, 33.8, and 26.0 percent of the observations were collected during spring, summer and fall, respectively (Table 6). Figures 9, 10, and 11 show the seasonal distribution of observation data south of the Sun River. Seasons are defined as above . Table 7 presents the 1986 observation data by type for each season, north of the Sun River. Table 8 presents observation data by type for each season, 1986, for the area south of the Sun River. Observation data north of the Sun River is composed of 67.3 percent radio locations whereas south of the Sun River 55.7 percent of the distribution data is from radio locations. Seasonal distribution maps reveal the importance of river valley, creek bottom and foothills habitat to grizzly bears during the spring. Schallenberger and Jonkel (1980), Servheen (1981), and Jonkel (1980) reported the importance of low elevation wet sites and creek bottoms to grizzly bears in the spring. The concentration of grizzly bears along these foothills, creeks and river bottoms appears to be related to the early snow melt from these sites and the phenology of important bear foods. Grizzly bears distribute themselves more evenly throughout the area during summer and fall. Several biases exist In present distribution maps. The study area is large and back country areas received less field effort. Much of the Information in these regions reflects a low intensity of field work, rather than the true distribution of grizzly bears. Restricted access to some private land also prohibited field work in areas which deserve attention. The Deep Creek and Harrison Basin area appears to receive high grizzly bear use; however, observation data are limited in this area. Another area deserving more attention is the Birch Creek-Lower Badger area west of Heart Butte. •19- ■'. v\ '"rn .? ■ ■■■'. « '-'-^ •• •. V . "^ A ]Chot*au 'Agiver^ Figure 6. Distribution of 1,273 grizzly bear observations collected during summer, 1976-86, north of the Sun River. -21- Glacivr , National \ Ctoct«r^^ MilM 0_J ^ Seal* '^"^'x* >-t7^..^^ \^r '▲AnuloiM /Chotoau Figure 7. Distribution of 898 grizzly bear observations collected during fall, 1976-86, north of the Sun River. -22- Figure 8. Distribution of 759 grizzly bear observations 1976-86, south of the Sun River. -23- Figure 9. Distribution of 305 grizzly bear observations collected during spring, 1976-86, south of the Sun River. -24- Miles 0 1 1 Figure 10. Distribution of 257 grizzly bear observations collected during summer, 1976-86, south of the Sun River. -25- Figure 11. Distribution of 197 grizzly bear observations collected during fall, 1976-86, south of the Sun River. -26- Table 6. The number of observations plotted on the Sun River South - overall and seasonal distribution maps, 1976 - 1986. 1/ Period Spring Summer Fall Total 2/ 1976-79-' 87 1980-83 57 1984 23 1985 71 1986 67 TOTAL 305 93 37 29 55 43 257 109 289 6 100 30 82 35 161 17 127 197 759 1 - South of township 21-22 line. 2 - Reported In Schallenberger and Jonkel, 1980. Table 7. Number of observations for each season by observation type, for Sun River North study area, 1986. Observation Type Spring Summer Fall Year Radio Location 33 Sighting 15 Scat 0 Track 13 Other 0 75 10 3 2 2 48 156 5 30 0 3 11 26 0 2 TOTAL 61 92 64 217 Table 8. Number of observations for each season by observation type, for Sun River South study area, 1986. Spring Summer Fall Year Radio Location 51 Sighting 4 Scat 1 Track 10 Other 1 38 1 0 4 0 14 103 1 6 0 1 2 16 0 1 TOTAL 67 43 17 127 Examination of trap site locations indicate the relative proportion of the study area sampled (Figure 12 and 13). Distribution data is poor in areas where trapping and radio relocation efforts have not occurred. Areas needing significant field efforts in order of priority are the Heart Butte area. Deep Creek area, and the North Fork of the Sun River. -27- Glactor . \ East NatioiMl \ GlMisr Park TWoMcdleltM MIIM 0 1 2 «▲ Antalop* ^T•lMI ">. '^i»«r^ Figure 12. Trap sites north of the Sun River, 1980-86. -28- Miles Oil Figure 13. Trap sites south of the Sun River, 1982-86 -29- Observation Records Data on grizzly bear observations including those from radio relocation were presented in the Distribution discussion above. This section presents the data on observations collected without the aid of radiotelemetry. From 1980 to 1986, 881 observations of grizzly bears or their sign were recorded. Bears were actually sighted in 312 of these. The type of sign recorded in the remaining records included 280 observations of tracks, 228 of scats, 38 of digs, and 23 observations of other types of sign including dens, hair, marking trees, and evidence of depredation, carrion feeding and predation. The number of grizzlies observed, either by sighting or from their sign, was determinable for 580 observations. Nine hundred-seven grizzlies or their sign were recorded in observations of from 1 to 7 bears (Table 9) . There were 56 records of the sighting or sign of grizzly cubs. The number of cubs recorded per observation was from 1 to 5 and totalled 116 (Table 10). The observation of 5 cubs was an observation in 1982 of 2 adult females with 5 cubs (1 with 2 cubs, 1 with 3 cubs) on Rocky Mountain. There were 40 records of the sighting or sign of yearling litters (yearlings accompanied by an adult female) ranging in size from 1 to 3. The total number of yearlings observed in these litters was 80 (Table 11). Table 9. Number of observations of grizzly bears by number of bears/observations and total number of bears observed on the Rocky Mountain East Front, 1980-1986. Number of bears/observation Number of observations Total number of bears 1 2 3 4 5 7 Total 387 95 68 26 3 1 580 387 190 204 104 15 7 907 Table 10. Number of observations of grizzly bear cubs by number of cubs/observation and total number of cubs observed on the Rocky Mountain East Front, 1980-1986. Number of bears/observation Number of observations Total number of cubs 1 2 3 4 5 Total 19 20 12 4 1 56 19 40 36 16 5 116 Table 11. Number of observations of litters of yearling grizzly bears by litter size and total number of yearlings on the Rocky Mountain East Front, 1980-1986. Yearling litter size Number of observations Total number of yearlings -30- 1 2 3 Total 11 18 11 40 11 36 33 80 The kinds of activities grizzly bears were recorded doing from the observations records were similar to activities reported for radio collared bears by Aune et al (1984) (Table 12). Bears were sighted most commonly feeding at a carcass, at alpine dig sites, in berry fields, grazing in parks, and while traveling. Bears were rarely observed while bedded or feeding in dense cover types. This is in contrast to activities reported for radio collared grizzlies by Aune et al (1984) , where radio collared grizzlies were more commonly bedded and utilizing food resources in timber and shrub plant communities. Table 12. Activities of grizzly bears from observation records, 1980-86. Activity No . obs . Percent obs. Feeding Activities General feeding Carcass or Carrion Grazing Digging roots Digging Pine Nuts Digging small mammals Tearing logs Tearing anthills Turning cowchips + rocks Turning over litter and duff Feeding on berries Anthropogenic foods 14 100 29 116 20 5 1 1 9 1 24 29 2.65 18.56 5.49 21.97 3.79 0.95 0.19 0.19 1.70 0.19 4.55 5.49 Non-feeding Activities General Bedded Traveling Mating and courting Denning-predenning Wallowing Playing 17 17 110 16 9 2 3 358 3.22 3.22 20.83 3.03 1.70 0.38 0.57 100.00 The kinds of habitat 13) was similar to ha al. 1986). However a component reveals a habitat component, statistically, it in the observation Rock/Talus /Scree, moui^ probably over repres observations recorded In contrast, 10.8 with little or no cove components used by grizzlies observed in this study (Table bltat component use by radio collared grizzlies (Aune et. comparison of the percent of observations In each habitat difference with the percent of radio locations In each Although no test was conducted to compare results that use of heavy cover types were under represented tecords. The use of open habitat components such as tain grassland, sidehill parks and prairie grassland was ted in the observation records. Forty percent of the were In habitat components with little or no cover value. of 1424 radio locations occurred In habitat components r (Aune et. al. 1986). appears en percent -31- Table 13. Number and percent of observations In each habitat component, 1980-86, Habitat Component No. Observations Percent Observations Cutting Unit 1 0.12 Meadows 17 2.06 Roads 2 0.24 Sidehill Parks 35 4.01 Snowchutes 6 0.73 Shrubfields 8 0.98 Rock/Talus/Scree 141 16.90 Closed Timber 186 22.38 Open Timber 53 6.32 Limber Pine Savanna 36 4.38 Prairie Grassland 99 11.98 Mountain Grassland 32 3.89 Populus Stand 101 11.92 Riparian Shrub 69 8.27 Riparian Complex 35 4.13 TOTAL 821 100.00 8072/2 The number of observation for each 5 day period from Jan. 1 to Dec. 31, 1980-86 was determined to examine the time period of observation and when bears were most commonly observed (Figure 14). Observation records are prevalent from the second week of March until the last week of November. However, one record for the month of February was available. The record of observations is consistent with data from radio instrumented bears regarding den emergence and den entrance. The largest number of observations by 5 day period was 36 during mid August. This corresponds with the time that radio collared bears were commonly found in open alpine areas digging roots and are thus easily observed. Home Range Annual home ranges were mapped and sizes calculated for 9 different grizzly bears monitored during 1986 (Table 14, Figures 15-23). Minimum annual home range size varied from 59.3 to 542.4 sq. km. for female grizzly bears in 1986. Two minimum annual home ranges for males were 599.5 and 805.2 sq. mi. in 1986. Over all years (1980-86) the mean annual minimum home range of adult males was larger than all females (F=15.62, P= 0.001) but was significantly smaller (F=3.08, P=0.10) than subadult males (Table 15). The mean modified minimum home ranges of adult males and subadult males were not significantly different (F=0.06, P=0.806). Subadult female and adult female mean annual minimum and mean annual modified minimum home ranges were not significantly different (F=0.69, P=0.41, F=0.17, P=0.68). The modified minimum home range of all males was larger (F=5.84, P 0.025) than for all females. Adult bear home ranges are probably a factor of habitat and reproduction. Adult female annual home ranges are more likely driven by habitat conditions with the female strategy to optimize the conversion of energy into progeny. The adult -32- c c r > c o 1 TT i r 1 « 1 l_ 1 O o 1 r. 1 t— Q 1 UJ ( T- 1 — *^ I • 1 — o ..J.. 3 t 1 < I r" 1 > f— 1 *— 7*> —J 1 r — 1 UJ {— 3C c: »__— 3 ^ — ~> 1 1 >- 1 < 1 y c c r « L a: a. < 1 4 E < 2 1 o i 1 o CM 1 O 00 I O 00 > o z I o »^ to a CO o •H M « in ^1 (1) cu -i o a (U u 0) c o •H U ta > »^ (U ca O (U c I n I U 3 00 Table 14. Modified minimum and minimum annual home range sizes of grizzly bears, 1984, 1985 and 1986. 1984 (km=") 1985 (km^) 1986 (km^) Mod. Mod. Mod. Bear No. Sex Age Mln. Mln. Mln. Mln. Mln. Mln. 335 F 7.5 — — — — — 435.4 500 F 6.5 91.3 559.3 180.8 621.7 198.9 423.4 313 F 4.5 45.6 195.5 52.9 127.0 144.6 243.5 366 F 5.5 10.9 95.4 60.2 128.9 84.4 190.5 466 F 15.5 — — — — 10.8 59.3 355 M 8.5 84.7 512.61 348.5 831.9 397.7 599.5 301 F 13.5 — — 117.5 336.6 87.7 317.4 316 F 4.5 — — 188.1 655.6 446.0 542.4 467 M 3.5 — — — — 168.7 805.2 Table 15. Mean annual home range size of sex and age classes of bears 1980-86. Mod. Mln. (km^^) Minimum (km^) N Mean S.D. Range Mean S.D. Range Adult Males 238.62 181.07 68.0-456.4 660.83 221.48 388.1-1000.1 6 Adult Females 158.89 90.43 10.8-288.5 382.11 160.59 59.3- 734.6 21 Subadult Males 263.97 191.18 71.6-606.4 1118.43 604.09 441.7-2055.8 8 Subadult Females 143.49 123.19 10.9-446.0 334.07 158.50 95.4- 655.6 12 male strategy for maximizing reproductive output Is to Include more females In his home range. Subadult males require no larger a portion of habitat annually than adult males (I.e. modified minimum range sizes are similar), but because of large exploratory movements have larger annual minimum home ranges. Table 16 presents minimum and modified minimum home ranges of bears (Includes all years data) . A modified minimum home range for subadults was not derived because subadult males dispersed so widely that modified minimum ranges were not considered valid measures of home range. Adult females and subadult females were pooled because no significant difference existed between home range size of these age classes (F=0.17, P=0.68 for modified minimum F=0.69, F=0.41 for minimum) . Aune et al. (1986) hypothesized that grizzly bear home range size may be a function of habitat quality. Jonkel (1982) stated that food and cover are major determinants of home range size and shape. Home ranges should thus be smaller in areas where food and cover (habitat quality) are better. Picton (1983) suggested that climate could predict grizzly bear litter size. This indicates that energy in a temporal sense can effect bear nutritional status. It is also likely that long term climate patterns which vary from place to place can affect long term spatial arrangements of energy. Thus areas with optimal climates for bear foods which can grow in abundance within a small area would result in small home ranges. In contrast areas with less optimal climates for bear foods which cannot grow in abundance in small areas but are more dispersed could result in -34- Figure 15. Annual home range of bear 316, 1986. -35- Figure 16. Annual home range of bear 301, 1986. -36- Figure 17. Annual home range of bear 355, 1986. -37- Figure 18. Annual home range of bear 500, 1986. -38- Figure 19. Annual home range of bear 335, 1986. -39- Figure 20. Annual home range of bear 467, 1986. -40- Figure 21. Annual home range of bear 466, 1986. -41- Figure 22. Annual home range of bear 366, 1986. -42- Figure 23. Annual home range of bear 313, 1986. -43- Table 16 Minimum and modified minimum home ranges of grizzly bears for years combined • Bear No. Minimum (km^) Modified Minimum (km^) No Fixes Adult Males 485 873.34 502.99 78 218 661.99 — 38 271 1709.13 1374.70 84 355 1084.45 872.75 94 282 1389.22 1097.73 75 346 1000.04 — 30 229 649.81 1052.57 — 19 Mean 962.04 S.D. 386.24 368.51 Subadult Males 467 805.19 — 27 333 26,672.00 — — 93 544 1747.63 — 72 498 2239.50 — 51 328 2300.07 — — 41 392 453.81 — 44 529 1366.39 — 35 326 2909.81 — 32 Mean 4811.80 S.D. 8869.82 Females 313 274.13 238.37 92 366 213.36 170.68 100 466 59.34 10.80 23 335 919.50 635.18 143 220 1022.99 713.17 258 548 385.50 257.00 48 273 528.30 342.19 249 301 552.34 342.83 53 500 890.68 496.73 154 317 391.66 195.83 52 518 379.56 257.12 53 316 827.68 512.09 68 Mean 537.09 347.67 S.D. 310.90 204.89 larger home ranges. In summary the spatial arrangement of energy available to bears could be largely a factor of climate, in particular precipitation, and would dictate home range size. In 1986 we examined two gradients in precipitation and the subsequent implication that habitat quality might be reflected in home range size. By dividing the area north and south along a bear management unit boundary we tested home range size in the Badger-Two Medicine Area with home range size south of this management unit. The Badger-Two Medicine Unit has been subjectively labeled higher quality bear habitat due to distribution of foods -44- and the influence of a moist pacific maritime climate (Aune et al 1986). Weather records substantiate the higher precipitation average for this unit as compared to the BMUs to the south which have drier climates and habitats. A gradient in moisture from east to west is also evident. Here we have used the forest boundary as a divider between bears. Using the geometric activity center of the home range of a bear we classed bears into north or south and east or west classes. An ANOVA was then used to test sex classes of bears by location (Table 17) . A distinct difference between home range size in the Badger-Two Medicine BMU and the BMUs to the south is supported for females and both sexes combined. A sample of only one male in the Badger-Two Medicine BMU makes conclusion in regard to males impossible. However in line with the supposition that females home range size is more directly linked to habitat the statistical test is supportive of a difference of habitat influencing home range size. The test between east and west bears in our sample was not conclusive. There was a weak relationship between females home range size west and east of the divide but not a significant one. It is likely that our sample from east to west is not along a large enough gradient to confirm the hypothesis. Home range size of females from west of the divide would be needed to make the sample span the full spectrum of this moisture and habitat gradient. Table 17. Comparison of home range size between classes of bears along precipitation and habitat gradients, 1980-86. Class N Minimum Home Range N Modified Minimum Ho Mean (km^) F-Value me Range Sex Mean (km^) F-Value Prob. Prob. Males North South 1 6 873.34 1083.11 0.22 0.66 1 5 502.99 796.21 0.29 0.62 Females North South 3 9 182.28 655.36 9.00 0.01 3 9 139.95 416.90 5.97 0.03 Both North South 4 15 355.04 826.46 4.90 0.04 4 14 230.71 552.37 2.81 0.11 Males West East 3 4 1222.31 926.27 1.01 0.36 3 3 916.81 577.87 0.78 0.43 Females West East 5 7 403.73 632.34 1.67 0.22 5 7 279.57 396.30 0.94 0.35 Both West East 8 11 710.70 739.22 0.02 0.89 8 10 518.54 450.78 0.15 0.70 Breeding Areas Seven individual courtship associations were observed in 1985. Bear pairs were observed in Debrota Creek, Crow Ridge, Smith Creek, Elk Creek, Landers Fork, Crow Creek, and the Two-Medicine Ridge between the dates of May 20 to June 17. Also female bear 366 was located near the capture site of male bear 498 in late June suggesting another possible association. No courtship associations were observed for female bears 500 and 313 in spring, 1986. However, movements of these bears suggest that both may have returned to area's where male bears and breeding activities were observed in previous years. Male bear 355 also returned to an area in which he had encountered females in past years. Data from 1980-86 has shown that all spring range is used during the breeding season and should be considered breeding area. In addition some female bears appeared to select some remote areas which are not considered spring range, to breed. Bears such as 301, 257, 335 and unmarked females with males 355 and 346 selected high elevation subalpine or alpine areas to mate. -45- Thirty-seven courtship associations of bears were observed from April 21 to July 15 during the period 1980-86. All but 6 of these courtship associations were recorded by radio telemetry. A total of 56 paired bears were observed in these courtship associations including multiple sightings of a single pair. The peak of pairing and most probably breeding activity is in late May with possibly a second pulse of activity in mid June (Fig. 24). The observed duration of courtship associations varied from 1 to 19 days. The mean duration of a courtship association resulting in a pair bond was 8.2 days (N=19) . In most cases radio monitoring intensity was insufficient to determine the actual duration of the pair bond. Our assumption is that radio monitoring probably underestimated the duration. However in some of the longer cases it is possible that more than one female was in an area and a male bear was associated with more than one bear during the monitoring effort. Activity Patterns Activity patterns measured on the Rocky Mountain Front were previously reported (Aune et al (1982, 1983, 1984, and 1986)). Aune et al 1984 discuss the hypothesis that there may be differences in activity patterns between bears in remote areas and bears in areas with high levels of human intrusion. To test this hypothesis we examined East Front bear data from 1979-86. Activity data were insufficient to test an individual bear within two different settings or during the spring period. However data were sufficient to compare groups of bears during the summer /fall period. Table 18 presents data from monitoring sessions conducted in 1979-86. Data from 17 monitoring sessions were valid for this test. We had to exclude sessions involving impact monitoring as the influence of disturbances would bias this sample. Sessions were also selected according to the ability to format data according to Garshelis and Pelton (1980) and to include as many different bears as possible. Table 18. Data from activity monitoring sessions 1979-86. No. Bears No. Sess ions Hours Monitored Aug Hr/Session 1979 2 2 36.00 18.0 1981 4 15 204.87 13.6 1982 5 11 105.65 9.6 1983 4 11 102.04 9.3 1985 1 2 56.00 28.0 1986 3 9 5 46 107.00 611.56 21.4 13.3 Ten sessions, involving 152 hours of monitoring on 5 grizzlies, were combined to represent the average activity patterns of lowland bears. Three sessions were included which did not involve monitoring of motion sensitive collars. However these sessions were necessary to give the sample a stronger representation from the daytime period. The data used was biased toward sampling of the dusk to dawn period as monitoring in 1979-83 was primarily directed during the time when bears were active and moving (Table 19). We do not feel that this bias caused a serious problem in this analysis. Most likely daytime activity may be underestimated but the pattern observed was real and matched those observed in monitoring sessions of individuals in this group not included in our analysis. -46- 00 I o 00 ON 3 I in ^ ~0 LiJ 3 K) lO < 2 fM f*» CsJ — o '<^J — SH iVd 'ON •H M CO o •H p. B •T3 U1 P •H -O 0) > U 0) (0 .a o CO u cd (U N N •H Vj bO O CO •H CB M-l O t-i CU •§ 3 I I (U u 3 •H 1^ Table 19. Hours of monitoring within each 1 hour sampling period, 1979-86. No. Hours Backcountry 7 7 7788776666667766777 877 Lowland 999999876422433446568999 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 Time (hrs) Seven sessions involving 163 hours of monitoring on 3 different grizzlies were used to represent the activity pattern of backcountry bears. All sessions included bears fitted with motion sensitive collars. Sampling was more uniform throughout a 24 hour period within this group (Table 20) . Table 20. Hours and levels of activity for two bear groups on the East Front, 1979-86. Prob. Activity 50% Lowland Backcountry Prob. Activity 50% Lowland Backcountry Actual Hours In Mean Sample 13.5 85.5 12.0 81.5 X^ = .0015 10.5 66.5 12.0 81.5 X2 = 1.19 Prob. of Activity Mean S.D. N 82.4 13.3 14 62.5 6.7 12 F = 21.25 20.0 9.9 10 26.9 8.7 12 F = 3.24 Aune and Stivers (1985) discuss the nocturnal habits of grizzly bears along the Rocky Mountain Front lowlands. In the sample of lowland bears a nocturnal activity pattern confirms previous observations (Fig. 25). In general nocturnal patterns have been noted in all bears while utilizing low elevations habitats along the Front (Aune et al 1982, 1983, and 1984). These patterns usually vary in length according to the length of day and temperatures. Activity during the daylight hours in these environments is generally confined to the dusk or dawn hours. Occasional midday feeding bouts in dense secure cover while berries are ripe have been recorded for lowland bears. In contrast to the lowland bears the average activity pattern of backcountry bears is crepuscular with peaks of activity near 0700 and 1900 hours. The actual activity patterns of individuals was variable. Diurnal, crepuscular and complex patterns of Interspersed periods of activity were recorded. In some cases as many as 5 distinct activity peaks occured during one 24 hour monitoring period. -48- c -9 rw ro - cd (U N N •H M 00 >s »^ c 3 O o J^ o cd ^ -a a td -a c Cd o o CO c cd tx >, u •H > •H U O Cd I There was no significant difference (P=0.90) In the average hours of vigorous activity between lowland and backcountry bears (Table 20) . There was no significant difference (P=0.25) difference in the average hours of moderate activity between lowland and backcountry bears. It appeared that both bear groups spent equal amounts of time engaged in vigorous activities within a 24 hour period, usually 10-15 hours. The average probability of activity of lowland bears was significantly higher (P=0.0001) than backcountry bears during vigorous activity. The average probability of activity was significantly lower (P=0.087) during moderate activity for lowland bears when compared to backcountry bears. These differences could be a product of the level of human Intrusion influencing bears, age and sex of the bear, or differences in habitat and food resources. Schleyer (1983) suggested food, cover, and temperature have major Influences on bear activity patterns. Lowland bears on the front were exposed to concentrated food and cover along cool riparian areas In higher temperature environments. They are also exposed to high levels of human Intrusion throughout the daylight period. It appears that lowland bears have adopted an activity pattern to accommodate their environment and human competition. Giest (1971) stated that, "mammals learn to minimize encounters with humans if harassed enough by reducing activity to areas, habitats and times of day where encounters with humans are minimal." Grizzly bears along the lowlands of the Rocky Mountain Front are exposed to many forms of harassment throughout the summer-fall period and are hunted during the fall. These pressures over time may have resulted In the evolution of activity patterns from crepuscular toward a nocturnal pattern. Andrews (1979) Indicated that shifts in "time territories" may be a mechanism for reducing stress in behavioral Interactions. Interactions between bears and humans along ' the Rocky Mountain Front can be a matter of life and death for either party. The adjustment of "time territories" may be essential for the maintenance of grizzly populations across the Front lowlands. Further study is needed to determine if adjustments are made in activity patterns during movements to and from the lowlands and backcountry areas by an individual bear. Also further sampling Is needed to reinforce data sets thus far analyzed. Information is also needed on the Influence of these shifts in activity patterns on energetics of the bear and its ability to access environmental resources. Food Habits Bear scats contained food items from 9 major taxonomlc groups including; mammals, insects, birds, trees (pine nuts), sporophytes, forbs (Including roots and corms) , gramlnoids, shrubs (fruit) and debris (Table 21). Bear food taxon were ranked according to percent frequency and percent volume which may Indicate food availability and seasonality (Table 22). Gramlnoids, forbs, and insects were the most common bear foods along the east front and have high percent frequency values. In contrast seasonally important or less common foods such as fruit, mammals, sporophytes, and pine nuts had low percent frequency values. Gramlnoids, forbs, and fruit had the highest percent volume of all bear food taxon. Domestic cattle and deer were the most common mammals eaten both in frequency and volume. Other large herbivores in the diets were domestic sheep, elk, bison, moose, and black bears. 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Oi OiH 0) -l a o 6^ U O • 4J tH \D o o C30 H > CTN r~. a\ »— H 6 o n B^ . 6 *J i-H cu u N u to N M P^ •H U 00 o rg O --t S o Vj u-l CO 4J r-l s CO (U h CO •H CO >> rH to (3 6 cu <^ 0) S 4-) to M 55 i-H Cv) (U iH 6 Pi J3 m o -* —I u-i CV| 1— I I— < in P-. o o o o omoou-lOo^r^\o lno••-l\oo^■NI■ OeM\C>00O-*— (tvj^ooN CN CVJ 00 CSI NO ONOOOn\OOOOn.-i CN'— tlOf^"— I'-HStiA C3N in o >* O O O ON >— I I— I I— < CS| oin>-iooNomr^ inoinr--'-'ooocM CM \0 00 -* o Csl -^ I— I vf O 00 00 NO o r-H r~ "d- CO ■— I fo r^ r^ r^ ST CO -* o -^ ON ON ON O ON fo 1-1 sr o o o o m m o^ r~« •— 1 r-» 1— I On O O O O O ON f— I 1— I .— I >— I I— I CNJ fO i-H •— 1 I CO CM \0 00 ^ ^ m NO I— I rH ■— I Cl •-ioomoN.-Hooin\o fO >— I CO >-i •— I m en 4J 4J 4J 4J CU CO to CO CO CO CO O CJ u U U O CJ ^ rH r-H iH r-H i-H CO JS X: ^ rH CO CO > >N U PQ M M V4 4J o 4-1 u 4J O 4J 4-1 «J 4J 4-1 4-1 O iH rH o o o o o H O o o H CU CO CO CO CO CO CO H N N H ^ CU e B 6 H l-l M 1-1 u u u u B R p CO CU CU cu CU cu oj N N O CO o o o Qi rO G b c ^ o S 6 e a 6 e ^ •H •H ,o CO M 60 60 60^ V (U cu a- si- sf «* -* -^r o o o o o o NO NO NO NO NO NO I NO NO I r-l ,—1 I o o I NO NO I r^ CT\ O O O 1 rH r-l Csl CM CM I O O O o o I NO NO NO NO NO csl o 00 00 I B o U td o CO u (U J2 N N •H U 60 O CM o e o V4 3 CO (U CO •H CO CO CM 01 6-S 0) •u 3 arH g 08 M > (U 4-) 3 D-.-I Fi CO M > (X E o 6-2 (J O 4J rH O O H > ^s (U o S 4J (U g 4-1 cd o o o o o o o o o o o o o o o o O O O O O — I o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o \o ON .— ( o o\ o o r^ O Csl o o o vO O 00 O O CTs O CO O O CO O O O O 1^ o o o o ^ m O O O O —I O CM o o o o o o cy> o o o o o o o o o o o o in o CM o o o o o o o o o o m o o o o o o o in m CM O r^ O O in o O <3> O St o r«- o m \D o O r^ 00 in \D r~» 00 o r- in — < in i-H 1-H o 1—i »* •* cTi on m — 1 en t-i ^ r-H 1— 1 CO \o \o in -H 1— 1 CO \o 1—) r^ o •-< 1— 1 T-i CO r-- CM 00 m CO CO -vT O O O • • »— 1 o • o • O '-<•*'-• CO ON o o o o o o • ••••• O o • CO * 00 ON CO O CJN 00 CM m r-. I CM NO I «* \D -H CM —t csl CM 00 CO m o CM CM CO CM m O CM O CM CM CO fO CM CM •* O O CO NO CO 4-) 4J o 5 o JS 'V p. B C O o O H rH o H td CO -H to O iH CU (U H u u Cd c t to P.,C (U CO TJ T3 0 0,0 4-t M u u u 43 •H -H ,Q ■H 'rj 3 o c c ^ c 3 td (U ^ S O H C3 C3 CO r-l e Pc; 1 CM CM CM 1 CO CO CO CO CO 1 NO NO rO cu pq 1 eg CM CM 1 CM CM CM CM CM 1 CM CM Cd 4-1 S 1 O O O 1 o o o o o 1 o o H M Z 1 NO NO NO 1 NO NO NO VO NO 1 NO NO I-H I ^ CM CM CM I O I O O O O I O I CO CO CO CO I NO I NO NO NO NO icostmvor^oo |.-h.-h lOOOOOO lOO ICOCOCOfOfOCO InOnO InONOnOnOnONO InONO 00 I e o u M-( CO *J cd o w u Cd , t-l td CM (U t-H ,£1 (d H 6^ 0) e Cd M > a. B o o o o H > B^ (U o 6 4J (U M 4J Cd M (U 0) S 4J Cd M jz; o o o o o o o o o o o o o o -d" 1— I O '-I ■— I ■-I 1^ o o o u-> I— I r^ O r^ C^ CS o o «* o o o o o o o o o o o o o o r~. \o o O o r- O O O O \0 "—I ON o ■— I o in m i-H o O r-» o \o O ui o o o o o o o o o m r-. >— I O O r-» ro CM ir> in — I fn in vo t— I o 00 CM r^ o\ o fo csj n o en O o en o sf o o m o o o o o m \o r-« r-> sr CN ^H CM n fO ro c^ m in o S3- ON O •—! CM 00 CO O CM 00 i-< .— I r-H CM r^ cjN in O CM CM r-l CM O CO PO o o o o O o o o o o o o o o o o o o o o o O o o o o o o o o o o o o CM CN CO r- <-H m \o \o m m o m o f-H i-H CM O fO ro ■^ f-H m o o in in I— I o CM CO CO .— 1 CM m CM fO m o o 00 .-I 00 o o o o ex. r-l rH .— I 1— I CO m CO o CTN ON «* o CM CO m >* CO m o r-- CJ\ \D CM -H CO r~ \o r^ 00 CM PO I— ( C3N .— ( i-H .—) .— I •* O O O O 00 CM CM ■* \0 o o o CM CM ro 00 cn --I --H oo 00 CM r~- <-* ro o o o o CO u •H pq -i "O Cd Cd .A o m pq cu O I I O S H H cd 4J o H x> 3 CO 4J Q CU X! 4-1 o o H I CM I O I VO I CM ro >a- 00 I o o o o I r^ r~. r^ r>- I vO ^ o B § cr u >4-l B CJ u a cu 0) H S C7 C7 a ^ 0) C7 2 C7 (U u PC, Ft. m vo o^ r^ 00 CM vo.*cjNOor~nHinc^ r~ O CO VO CO O .* to H O <^ r-~ CM CN CM CO in o vO CM CO in 00 CO CO CN ^ ^ CO VO -* 00 O 00 00 CM H CM <3N C3 C3 H O Jf o VO r~ H CM CO m cor~-i^HHcT>vo-* -* in CO CO r^ o O CO O CO • • H CO O z m .* r~ CO H 1 CO 00 H 1 CM CO O H • • o vO on CJv H CM H CO O CO CO o o O CO CO o o CM CM in CM f^ o o 00 CM O vO 00 o in CM H o o o CN CM 00 « B •■-1 H-1 S M n Oi CO ■B o. O CO o u c^ o CO Ct< m U -rl Vi M 3 4J CO cu J3 c •H CO R (U •a CO (U N N •H 00 00 \o e o cd CO o CM CO H M CB • (U o m z 1 •H 13 c B o O •H U U • CO u >> "O • . i-i H 4J CO u •H CU ,Q p. CO >. W H a> ft o e^ r-t CO 4J u (U o. /'N CO o >-' 1 CO > C » CU H Q B O •H 4J (U CO 6 O CO O \z hJ c • (U o o 5a fO CM o o o o > > O B BBBBBBBBBB cMor^ ^ocoooco— iOAl^^A!4!=> P !=> COCslfOm CMIO O'O'oaJ B'OBBBTJTaTj'a'a'oaj "ooj oj qj 'O'DTJa) 000>B;!iJO^Ai,i<1000000>BO>B>fi>BOOO> OOOCO-HBOBBBOOOOOOCOTHOCd-HCO-rlCO-HOOOcO B O •r( O o CO MM > M M > > > o o u Cfl Cfl H << > o in r-- in CO WW o o w in o o in CT\ r-~ en «* St CO CM «d- CO !z; iz iz K Z 2! fO CM o \o CM CM r-~ t-H \o (yi f— 1 1— 1 o o O M o O CM CM tH CO U s CM CM •H > CM CM 60 t>0 4J CO (It <3C bU 3 3 CO O 3 3 3 P Q ia a Q O -,'V 3 O -H a 33 W SflCMICOl M CM CO M M ^ CU 0) (U CU CU CU M )-i M CD U U Q> U 3 tm Pi m CO CO > > foicoini ■* m \o « M M CM CM M M M OOMMM O COMMMMM CMCM>>>>>>>>>> O U O CLJ CJ W U CO CA cn CO c» Fi( cn < > > > > S > o CO > HjJJWWWJIlWWWhJ MMMWWWMpqWWWM Ph PM PL, X X X Ph < >< X >oin-d''^'>D»3'\o\ovO'vO W £3 W W W W wwwwwwoooooo oooooocMcyi»a-s3-.d-<-i cMCMr^cMin-jf"— 1»— 1>— ii— irHi-H Z!z;ZZZS:wcococ«coco \ofnnco-H>— i>-io mr-~r~.r-.ror-in\or^p~r^sr CMOOO— lOCMCMfOcnoOfO CMCMCMCMCMCMCMCMCMCMCMCM tjOetobObOOObObObObOCiObObO 333333333333 QQQQQQannQQO CO CJ o >-i CU CO n 3 CJ cr •O AS CO o CU "rl CO 4-1 ^ ^ A! .^ .^ »4 S CU CU CU CU CU CU^^ 'H OrH«H»H CO CO COM SW»iJCk:;coSS;3!3!3co 4-> CO O 00 CU u cd H ICO |M |M I—, ifo i«a- isrisi- isr I-* isM r-.ooo>o—icMn-*in^or~oo CM CM CM CM O O O ,Q M to 00 O 1 CM CM CM > > > M CM CJ CJ CJ CO CO CO <; > > <: tj hJ J hJ < ~- CU 2:^ «* m in 1 W w w o o o w w w o o o CM o ^o o o o \o r-. St CM CM CM d- m SO m o «* 00 in fO CO 00 in in r~. .— 1 .—1 CM i-H M O CM CM f— < CM CM CM CM CM CM CM CM CM 60 00 60 3 3 3 P Q P CU u CJ 60 J-i -H CO >( W 5: fOlstl CJN O r-H CM u o pj «ni 60 3 P 0) CU M O CO > ■H cni CN CM 60 60 60 60 3 3 3 3 P P P P ^ M H (U -H O U CJ Q> CO B B CU B Pu CU B 4J s CU 4-) 3 o pq s CJ St 1st 1st ISI- 1 fo St m \o CM CM CM CM 60 3 P (U (U u CJ 60 •H sti CM 0) 3 a •H U C o o 00 I as IB (U >^ CO 3 0) c •H ■C 4-1 •H CO c cu U ta N N •H »^ 00 C» SO e o cd CM cd H h C8 • CU o FQ Ja 1 X) c C o O •H U 4J • CO VJ >^ -o • (U O 10 z & -o CU c a CO >. ►J H 4-) Cd 4-1 •H CU ,o & Cd >^ IB H B (U O i-H •H U 4J (U a c >. 0) H o c o •H U 0) CO S u Cd o a l-J c • M O O u-i \o 00 --I o w w o o o CM <3> fvj CO |x] iz ^ 00 o m «d- 1^ .— I O •— I CM CM CM oofonomoomom f<^eM^~^>o^oo^oocMoo CMCMCMCMU-in«a-^eM MOBOOBBcd M 00 00 I t> <-H 1— I CM .-I O M M M 00 CM > > > -H 1-H r-< CM CM cn M <—l 00 00 M O M 1 00 00 1 M M 00 ^ ^ > i-H t-H > > -H u u u O U «J U U U U W «J U W CO c« to w crt W CO en CO fe CO CO < < < > > > > > > > > ^^^ > "^^ ^''•»*. 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B 6 Cd Cd > B O u t-H Cd 4-1 00 • •H ,ii Cd fL, u 4-1 PJCJPQUWOCOCO iri im IPO im I ml POI mi -HI -;r i«a- ia-«*sj--*-d-si-si-mmmm * « « 1 ^ 3 *j CO (U 4-1 CO B M Cfl N N •H 60 00 \o B o CO o esi M to • (U o pq !Z 1 •a c B o o •H u -u • CO u >^ -a • . to 4J •H (U 43 ft to >^ X H 0) ft| o CO o ft/- tn o w .u (1) ft. B {>, £> CO <— I CO m CO ro CO B B B B B ^ A! J«! 4»i J^ B B B B B to ti & O t3 B CO rH o r^ ">0 \D CO —1 SO ,V! I— ( o o so \o t— 1 -< o \o B CO CO ir> «*■ CO CO CO CO <• t3 'O T3 T3 Xt "O -O xt tj (U 0) 0) Q) (U o o o o O O O O O CM CM ^ CO CO O O 00 00 00 CM CM "-H .— I i—t O CO I I I I I M CM M O M I I CM > u o CO hJ H tJ O 9 H C^ CO r*! U < < > X! > ^ ;3 ^ '^ ^^ pq X ^ M W M *^ •^^^ >. 2^ ^ < (U :^ -< CM CM 00 CM ■-I CM CT^ CM CM CM CM .-H CM CM \o m CO o o u-i m o in o o o CO in >* vt- sf \o CO 00 00 in tT> i s B 00 00 00 00 3 3 3 3 Q Q Q O • O 00 3 P Z o VO O O O CO o m CM rv g; •-< CO CM o o o o o CO \0 CM CO 00 CT\ in m m 00 .-H r^ 1^ r^ \o 00 00 00 00 00 3 3 3 3 3 O Q O O P m CO o o CO o o o o o o >* o o \o 00 r-» to u 3 00 00 4-) 3 3 to P P Z ^0 A! IH 4J fn 4«i B (U U a) iH !>, to > 2d CJ 43 O •H PQ (U > B O •O 1-1 > ,s r-l B 4J iH OJ iH -H B -H B 44 CO ^ 0) S o (d 43 CO JS O O " pq H o o 1^1 r-l ^». ---. — -^ ~s. --^ -^^ in I ml —I I"-! I-— I ii— I I.-I rs^ ~^ vi- m \o 1^ oo-ii i-*i m m m m m o\ o m \o •-H CM CO sr m \0 \0 sD so \0 VO r^ I so I B SO (U CM o T) m -a • (U B O e CO 00 to CJS u CO m i-H 0) iH T3 ft 42 to o (U ' i • B to iH O to 43 . B a "0 44 4J U O X) T* Xi •H > >J 00 OO-O 0) iH to 4J to 3 M to -O -a M TJ OJ 44 a p > •H ft « O to O i-H c >^ > CO 43 -H -H N •H 43 B ft 44 CM 44 N CO *H 10 CO OS to •H •o •a a) n o CO o M u 0) M T) 00 o o O, 4J 44 CO B O iH CO iH u CO 3 44 U o CJ B O O B to B ft OtUV443(UCUa) CM (U hJPO^PPQP ^ P!i CM 1 r 1 1 1 1 1 r~. 00 o so * — icMcosrmsor^ oo Figure 26. Den sites north of the Sun River, 1977-86. -68- Figure 27. Den sites south of the Sun River, 1977-86. -69- not significantly different (65°, N-12, P=0.25) from the mean east of the divide. These findings show that grizzlies east of the divide use northeast aspects while grizzlies west of the divide use southwest aspects for denning. Because northern aspects retain more snow depth than southern aspects and snowfall east of the divide is less than that west of the divide, the above findings would be expected. Gillespie and Jonkel's (1980) data on den elevation were also combined with our data to_ compare den elevation on each side of the divide. Westside dens were lower (x=1977m, P=0.j)005) than eastside dens (x=2164 m) . Den elevation in the Mission Mountains (x=2124 m) did not differ (P=0.10) from that east of the divide. All dens in the present study were dug except four which were natural cave dens. Three of these were found in one area. Two of these four dens were known to have been used by grizzlies. Three dens in our sample were used more than one year by the same grizzly bear. Seven dens were in an unusable condition the year following their original occupation. For all grizzlies den entrance dates ranged between October 14 and December 5 with a median date of November 8 (Table 24) . Movement to dens occurred from October 6 to approximately December 1. Emergence dates ranged between March 10 and May 13 with a median date of April 10 (Table 25). Bears in the Mission Mountains moved to dens between October 10 and November 20 and denned between November 2 and November 22 (Servheen (1981)). Den emergence occurred between April 12 and May 9 and den entrance between November 2 and November 26 in the South Fork of the Flathead River (Gillespie and Jonkel (1980)). Adult males and females with yearlings or two year-olds emerged from their dens (median = March 30) earlier than females with cubs (median = May 1) and subadults (median = April 13). Pregnant females entered their dens (median = November 5) earlier than subadults (median = November 8) and adult males and females with cubs which entered on the same median date (November 18). Impacts of Oil and Gas Activity No oil and gas wells were drilled in 1986 and no seismic exploration was conducted. As a result no work was accomplished in this area. The reader is referred to past annual reports for data and study results regarding this topic. HABITAT STUDIES Bear Management Unit Constituent Elements East Front grizzly bear habitat was divided into 6 Biological Evaluation Units in 1984 (USDA). These units were modified in 1985 and constituent element maps were created for two evaluation units (Figures 29 and 30). These units were renamed Bear Management Units (BMUs) for better interagency communication (Young, 1986). Constituent element maps for the remaining 4 BMUs were created in 1986 (Figures 31-34). Constituent elements were defined as spring, denning, summer, and fall habitats according to the U.S.F.S. (USDA 1984). Summer and fall habitats encompass the ■70- -9 ^ ^ CO CO o CO R CM O <* CM O CM ^ S^ 00 I U O 00 0) 4J u o (U CO to ^ 3 00 •H I 00 I o 00 CO (U •H rH N N •H u 00 !-i O CO C (U 13 U U c -i *-> CO c (U (U >< 6 0) > o € (U M-l Wl o < CO •H 4J O 3 •a o u a (U u u c w Q CO 6 •H X o (X 3" U u c c CD CO C n bO bO cu cu u >-< i>j B ft ft 0) CO >N >^ cu iH iH u ^ J3 ft •H •H CO CO CO 4J .U u u CO 4J 4J 4J 4J CO x> c c c c o C c c C 0 3 (U (U (U 0] ft cu 0) cu 0) ft CJ CO CO CO CO CO CO CO CO •o cu 4J 4j u u -l (0 B CO CO B cx a CO CO X .JQ c n 3 3 p- ft CO c CO ft CO CO CO CO ft a a ft ft X CO 3 ,0 3 X -H 3 rH CO CO 00 bO O U CO m 60 -O CO 00 00 00 bO CO CO CO 0 -a a a vj ^ XI (U ^ U 1 3 U U 1 ^ M 3 1 1 3 3 1 1 0 u 1 0 1 1 1 0 0 \o \o > \o NO 0) > > > 00 00 CM 0 CO CM CM 0 in CM CM 0 0 0 0 I— 1 r-H 1 Z ON 1 0\ On ON On 1 1 Z -I 1 1 1 z z z fO 1 1 CM CM 1 1 r-- 1 1 1 1 m m 1 1 m m r~-. 1 1 lo m CM CM CM eg CM c^ * 00 CM -H m CM CM m m m m m m ID •—! —t CM 00 --H CM m 1— 1 CM CJN CM CJN CJN CM CM >-i >-i ^ ^ p ^ M M M U M M U u u )-i h ^ ^ u u ^ Vj M M U u u u (U (u cu (U cu (U 01 P 0) (U CU CU CU -l U XI XI XI X ^ .jd ,9 5 .£1 ,Q ^ ^ X X cu X X X .fi rQ .£1 X X .0 ,J3 ,0 0) X X XI X X 01 0) 0) ess S B B 6 o B S B 6 S B ^ B S B S B B S B s e g X B B e B e x X X 0) (U > > > > > > A! > > > > > > w > > > > > > u > > > > 4J > > > > > u +J 4J o o o o o o o C o o o o o o 000 0000 cu 0 000 CJ 0 0 0 0 0 0 0 0 z z z z z z z 00 E3 z z z z z z 0 z Z mber 1 N mber 1 N N N a Z Z Z Z in gj 0 z z m •-H CU z m u 0) z z 0 0 0 \o CM i-H > 0 cu > 0) > cu > ^ ^ CM 0 0 CO 0 in 0 0 in CTN CJN —1 d- «vr m CM «* -H CM CM CO 00 ^ 00 i-H CM On 00 00 CM -H CM CO »— 4 »— 1 — 1 00 -H CN 4J -^ CM +J CM CM \0 >— 1 •— 1 CM CM CM CM CM 00 CM CM CM CM i-l O o Vi u u u u u U u I-i U U u M »-i n o M >J O ^1 OJ cu J Q) U }-< 0) CU »^ >>< CU M OJ OJ U U U (u cu cu cu cu ^ •2 -fi B ,0 .£> B B rQ JQ B rO B B ^ .0 .£1 O O 0) O O (U o cu (U (U o > > 4J > > > 4J 4J 4J 4J 4-1 > 4-> > 4-1 w > > ^J 4J > •p > > u 4J u o o m O CJ <+-! o o o o o o o o u u u CJ CJ 0 u 0 0 000 0 a 0 0 0 0 0 a 0 o o * ON r» -* CO m 00 CM • • • CO m 00 CM CM m 00 CM NO 1— ( r-l '-< CM CM .-1 1— 1 1—1 CM CM fe fe S pC4 pL4 pE4 p^ S (X4 fe h li. 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PQ pq B (U to 0) u (X 3 o B B & £M CN o O r-H O .-H 1—1 1—4 r-l u r—t ^1 M u u > > o o o o o o u J? z ■ t3^ CTi i-H I-H 1 «a- 1 cyv r^ a\ o CM «S \o CM \0 CM CM *4 u »4 !-i u U U 0) u u u M >-i (U u o > u 4J 4J *J > 4J U O O o o o o O CJ O O Mh o o \z !Z5 o o o o z O 4 M U CU ^ (U (U > > > (U > OS o o o o o o fsi cy> 5S !2! -* z -* Z 1 z 1 CM 1 1 I—* 1 rH 1 O -1 1 0\ ON 1 sr 1 0\ r-t cy> r^ CM -d- CM CM ■vO CM VO CM U CM rH U U V4 M u u Vj »H ^ M rf3 ,i3 .C ^ B rQ ^ o o O o o o O O CU o o 4J 4J u 4-1 4J 4J *J 4J > *J AJ o o u o o o o o o o o o o o o o o o o z o o m m m m \o \o so \0 so \o \o 00 00 00 CO 00 00 00 00 00 00 00 0^ C3> i-H »-( r-l a. t-H ON <7N 0\ 0^ 0\ rH rH rH rH rH m in lO «o uo IT) m IT) m m m CO \o r^ CO CO >-H to •* r^ u-> rH CO r^ f^ Pu Pm l±4 p-^ Pc< pi^ PC4 P* ■ a o. cd 4J 4J 4J *j P CO (0 c c w 0) ,£5 J3 0) (U to 3 3 CD CO (U 0) o o (U >4 >J »J •H a bO bO ft ft +J (3 C O CO •H -H CO CO 3 ,0 rH iH rCl JH ■o s >-i U 3 3 O u fH >H U CJ 4J (U 1 c 4J o (U •H 00 a en OV (U 1— < > c o X a o o w a M ft (3 -o ft cu c < a to cu o c - cu c (U TJ cu <4-l W) o < CO cu 4J X cfl (U a c« • • CM o cu iH M ja to to (U H PQ c c (U ^ tw O 2; I cu tn cu U ft u 4J C C CO CU cu ^ w CO 3 0) H O 4-1 c 09 % •rl U <■ m CO ft •sT I-l rH S in - 1 a\ CO \o CO 00 «-H 00 CM 1 1 o 1 1 1 . 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(U Pi C 4-1 OJ -H S Q (U 0) o c 00 s Cd B ■H o p. c p. l ^ <: S <3 S m m u-i o i-H 1-H 1— I CM ■H J3 .H J3 ^ >4 ^ >-i -i o (U 0) •o cd 6 0) cu 00 l*-l o I in I CM o 00 I I 00 B e 0) 4J B 0) 3 4J •H 4J n C o o ll 00 in >0 00 i-< CO (T> in in CO n ^ S 0) 4) U O g 2 111 >jl 111 .— . *^N •— \ Q ^^ y-^ ^-s H m • o vo in • • o • • • «0 00 O O vo H ci H i-l CM in es O Em I'll o CO 4J O H Ov r- o <^ H o -* CM CO CO CO oo in in in -t VO • ••»•■ H -* <(• CM ^ r-l 00 ov o m CM ov H CM CM CO ^ O CM ^ OO -* t^ VO CO 00 H CS ^ H in H CO m o 00 vo H • «•••• Ov H 00 vO Ov r~ in H O CM CM CO t-l CM CO H •* H 4-> ^^ ^-N rf—S ^^ ^^ ^^ CO CM vo O oo CM H « • • » • • U O o O o r^ CO ■* ~ " ~ CO «n o Cjv Ov vo B • • • • • O o H o CO in 2 I-l /■"s ^— ^ O *■**» i*^* ^"^ CO o^ • C^l 00 O^ • * O • • • c^ o^ o CN] »jD in CT^ c^ H Ch o cNi o c\ r*- ir> Ov o CO vo in H H t3 m H o H H CO S JjFj r-l o r~ oo r~ i~- -* e CO al BMU Are al Spring u tx 4J 4J U • « (1) Ix 0) »- o O O •o u > O H H H 1H s « 1-1 od M H Xi Pd 1-1 O o o ^ o u § § f w 4J 4-1 1-1 CO J^ CO B B B E m CO »4 . Sldehill Parks 8 3.4 _ _ Snowchutes 2 0.9 _ _ Shrubfields 9 3.9 •mm _ Rock/Talus/Scree 21 9.0 _ _ Closed Timber 44 18.8 22 23.0 Open Timber 42 18.0 20 20.8 Limber Pine Savanna 10 4.2 3 3.1 Prairie Grassland 3 1.3 Mountain Grassland 1 0.4 _ _ Populus Stand 45 19.2 22 22.9 Riparian Shrub 37 15.8 29 30.2 Riparian Complex 7 3.0 . _ Missing Records 3 237 1 97 Table 28. The number and percent of activity plots for each feeding and nonfeedlng grizzly bear activity type, 1978-86. Activity Feeding Activities Gen. Feeding Carass or Carrion Grazing Digging Roots Digging Pine Nuts Digging Small Mammals Tearing Logs Tearing Anthills Turning Rock and Cowchlps Feeding on Berries Stripping Bark Non Feeding Activities Bedded Traveling Dennlng-Predennlng Unknown Missing Records No. Sites 5 12 56 34 26 1 22 12 9 42 1 58 10 1 8 3 300 Percent 1 .7 4 .0 18 .9 11 .4 8 .7 0 .3 7 4 4 0 3 0 14 1 0. 3 19. 5 3. 4 0. 3 2. 7 -84- Table 29. Elevations of activity plot records, 1978-86 Elevation No. Sites 4000-4500 26 4500-5000 55 5000-5500 49 5500-6000 47 6000-6500 38 6500-7000 36 7000-7500 31 7500-8000 8 8000-8500 7 8500-9000 2 9000-9500 1 300 Percent 8.7 18.3 16.3 15.7 12.7 12.0 10.3 2.7 2,3 0.7 0.3 Population Biology A decline in field emphasis from the Deep Creek to Birch Creek core study area occurred in 1984. However, marked plus observed data from grizzly bears was collected and produced a seventh year of population data from the core area. Lower intensity of field effort probably reduced the reliability of data in 1984, 1985 and 1986 as compared to previous years. Some assumptions were made regarding previously marked bears on the area. Sex and Age Data Table 30 presents age and sex data from the marked population within the core study area (Deep Creek to Birch Creek) during 1986. Since 1977, 35 individual grizzly bears have been ear tagged in this area (Appendix C). Twenty-eight of these have been radio monitored, 3 were moved off the study area, and 13 are known to be dead or removed permanently from the ecosystem over a ten year period. Table 30. to Birch Age Creek, and sex 1986. data from the marked grizzly bear population. Deep Creek Adult Subadult Yearling Cubs Total Male Female Unknown Total li/ 3^/ 0 4 2 3 0 5 0 0 0 0 0 0 0 0 3 6 0 9 - No evidence could be found in 1986 to indicate presence of marked bears 2/218 or 203. - Excludes Bear 548, 220, or 257 since we could not verify these bears presence in 1986. -85- Table 31 presents age and sex data from the marked plus observed grizzly population from Deep Creek to Birch Creek, 1986. It is likely that more bears exist than were observed on this core area in 1986. Little field effort was focused in this unit and more subadults were present but could not be clearly separated by color marking or other physical features. Several adult bears expected to be present in the area were not accounted for because little trapping has been conducted in this area since 1983. Table 31. Age and sex data from marked plus observed grizzly bear population, 1986, Deep Creek to Birch Creek. Male Female Unknown Total Adult Subadult Yearlings Cubs Total 1- 6 1 8 2 0 0 5 5 0 6-' 3 9 14 26 - Lower field effort reduced efficiency of observing adults. In 1984 we observed two different adult males and eight adult females. It is likely that 1984, 1985, and 1986 figures are lower than expected because we spent less 2 /time on this area. - More subadults probably existed than could be easily distinguished in 1986. We count only those clearly identifiable to avoid duplication. The average number of bears observed in the last seven years is 28.6 (Table 32) The average number of adults in the area has been 9 and appears to be stable. Table 32. Age structure reported for Deep Creek to Birch Creek core area. 1980-86. Adult Sub adult Yearlings Cubs Total 1980 8 6 6 7 27 1981 9 8 7 2 26 1982, 9 11 2 11 33 !c^?*l/ 11 4 8 3 26 1984,i' 1985, 'Vj 7 7 3 15 '\y 33 29 1986 8 7 5 6 26 Decreased field emphasis in the core area reduced reliability at upper end of population range. It is likely more bears exist than indicated in this table. These numbers represent a minimum count of distinguishable bears based on .marked and observed animals. - These data were modified from that reported in Aune (1985) to reflect the 2/discovery in 1985 of three young for bear 335 in 1984. - In 1986 records indicate two females with 5 yearling cubs on Rocky Mountain apparently not observed in 1985 (one with non functioning radio collar) . If adjusted there could be 9 females and 5 cubs and a total count of 36 bears present for 1985. -86- I I Density Estimation Density estimates were calculated for 1980-86 in the Deep Creek-Birch Creek area. A major problem encountered in density estimation is determining the area used for the population estimate. Servheen (1981), and Aune and Stivers (1985), used composite home ranges for determining the area of analysis. In re-evaluating densities of bears on the East Front in 1985 we examined influences of subadults on outside polygons and the effects of habitat on polygon shape and density estimates. Three different polygons were developed using composite data from all bears captured and monitored from the area 1977-85 (Figure 35). The largest polygon (Area 3) is a simple convex polygon from all radio monitored bears. The second polygon (Area 2) is the outside polygon for all adult bears in this unit. The third polygon (Area 3) is a modified polygon with 98% of the radio locations of adult bears included and exclusion of nonhabitat areas along the mountain front which would otherwise be included in the analysis area. Table 33 presents results of density estimates using each of 3 analysis areas and evaluating densities for developing a minimum marked population and marked plus observed population estimate. Results indicate that analysis area 3 is probably too large an area for population analysis and is not a closed area because subadult bears widely disperse into surrounding areas. Area 2 in this analysis may be a better estimate of the proper analysis area but Includes significant prairie and farmland area not utilized by grizzlies along the East Front. Area 3 probably more properly estimates the actual area used by bears monitored and observed in the analysis area. Data from the three analysis areas also indicated the extent of emmigration from the core area to areas outside. Of all the bears captured outside the core area (in the areas to the south and north of it) none have Immigrated to the core area. Given the highly observed emigration and limited evidence of Imlgratlon by radio monitored bears, the consistent observation of unmarked bears in the core area, and the evidence that all bears in the area are not marked, it is unlikely that the population is at the minimum estimates presented for 1980-86. A more accurate population estimate would Include the marked plus observed animals. Using these animals and analysis area 1, a density estimate of 1 bear/51.9 km^ (20.0 mi^) is calculated as an average for 1980-86. This is very similar to density estimates of 1 bear/57.5 km=^ (22.2 mi^) in fall reported by Aune et al. (1984). Spring concentration of grizzly bears may double densities of bears along the East Front spring range. Densities for each year ranged from 1 bear/44.5 km^ (17.2 mi^) in 1982 and 1984 to 1 bear/56.4 km^ (21.8 mi^) in 1981, 1983 and 1986. Density estimates were calculated in 1986 for the marked plus observed population. Highly visible marks were not placed on each animal and marks were also lost. Our data only allowed imprecise estimates of the minimum - maximum marks present on the study area from 1984-86. Because new marks have not been placed on animals since 1983 our population data from the core area has become less reliable. Our Inclusion of data from this period 1984-86 In all population tables is to demonstrate the minimum information available for those years. -87- Figure 35. 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CJCje)T3UU''0'''0>J h >Jh • CI V^IO^^V^h-HU u -uu •^^&SW43^^r^omcJOCJ^< »J KUOCIi-fWrHiH -HtJ. gUdlaU -H-HIO tOtO^Vh^hiHtOl^ „H-0 OO >->>>>« P,UJ tnQ)iHOOIOI-HH(J T3*J4J4JiHTJrHrHT3*J»-) ^413 0000-Hnu-Vt3\OOOOOOOOOOOOOOOOOinu-imvOvOVO^C^O » » c c a G O O 0) U CI CI i-( r-i CI o CI a CI c c c c B B E c a B B B E E B B E E B B B B B 0 B CI 01 CI CI 01 01 01 CI CI 01 01 CI 01 CI 01 CI 01 01 O CI U 01 CI o 01 CI 01 CI CI 01 01 01 CI CI o 01 01 01 01 01 01 CI 01 O CI 01 01 01 01 01 IJ h iJ b u b I-I ^^ u M u I-I ^4 1^ u M u u IJ I-I U M U u u 0) 01 woooooooooooooooocjoooocjoooooooo .***^^-*~■•^0^■--^■--^^oOcoc*lcocnf*^fOcn^n^nfn(n^o^o^Of^fnfOc*l^oc^ ifn-*lOO— *•cr•^<^v:^■(U(U(U— (i— lrH(U(U(UQ)(U'*0\£>~«C)^£) n oinoooooooomu^rooooooofom ^-llnocJOf^OfOlnmcNeN\omOfOl^l0^o^^ iinomo mooQOO oo f^ocsio r^foooo CO I r .... I .1 -lhrHI-ihiH}-l»-lrHrHhi-tf-li-tl-<)-l m o O O O -H 00 m o o m o o ^ \o r^ •— < — < Cr\ *CMOm^\0 .r^r^t^cocMCNincM I C C C C B C itUQJtUtUtUdlVtU .^^^ — ^-.*-^o m^^^^ \£)\0\DSDmu^tACN ^ *d- ^ -* en <}■ B C C B E B Q) QJ (U Q) Q) r>- ON T3 rH B CO * 4J JS B u O 00 M B fe (U iH 4-1 (0 (0 CO ^ CO (U 60 C CO M 01 o -a- to CO <: m CM r^ CM CTi CM CJ\ 00 -- CO \o m CvJ O O "-H 1— I CTs O CO CO 00 00 00 Cvl 00 m m m m IT) m m I I vO ~a- to 00 o CO to vo in m •-! P-- 00 m m cvj CM 00 o in 00 vo m o •-< CTv CO CO r-. CO CM 00 o CO i-i \o \o r^ r~ r^ fv, 00 00 00 CO CO CO 00 CO I O r- cy. CO CO CO C M-l O O -H O srcMvoc?\r^cMOooo\o cO'-icor-^cMvooom-Nfco .-H >-( 00 J CO 0) M CM CO m -* r-> vo P^COvOvDCT^-*OCMcOOO COCMCM ,-lc\lCM.-lrH vf] 3 00 60—1 <; w . o I I I sasfessii-si* I CM 00 C5\ •vT 00 £> -l X cu •H 4-1 Tl c c N cu •H CO U v*^ O < J= U O CO •H cu ,C •o O. CO 4-1 M CO 60 O cu <0 60 o < CO ^ Table 45. Mean home range areas for black bears in North America.' Home Range Area (km'') Adult "^ Study Location Male Female Reference Alaska Alaska Alaska Arizona Idaho Idaho Washington (Island) Washington (Mainland) (79-100)" 153 (4-611)^ 141 (41-341) 29 (15-69) 105 (61-156) 112 (109-115) 5 (2-13) 61 (13-87) (10-30r Modafferi (1982) 117 Miller and McAllister (1982:98) 21 (4-46) Schwartz et. al. (1983) 18 (10-30 LeCount (1977) 18 (12-26) Reynolds and Beecham (1977) 49 (16-130) Amstrup and Beecham (1976) 2 (1-4) Lindzey (1976:39) 5 (3-6) Poelker and Hartwell (1973:72) a b c d Adopted from Schwartz et al. (1983) page 77. Age greater than 3 years-old. Includes all age classes. Includes all bears greater than 2 years old. -114- c o •H *J •H XI B O U *^^ »— < rH o O— ' »— ) O O O O p* TM 'oxfcc'O'occcc'a •O OT3 O O^^ O O ^ M M Jai O OiHOOCCOOCCCCO OOOOOt3t300C5!=)!3l=>0 u to • tl o PQ ^ • (» >^ >H tS (U • (0 u £3 (U Pi •o (U c a td ^ ►J H a. K H (U a o H CO 6^ • o ^^ \o 0) o 00 1 tn s-^ 00 to (U 0) iH ^ ClJ ^ o to -. — tOOCM'-HCMO'— I csiiommiTiinmio r-H O O — I .— I i-H I— ( t> ■— < CM CM I I I I I > I pqwOTpqwpqpdw F^ Ph en movoooooomO'-HOOo S ^ ^ & !!S & owwwow owowoow u-lOOOxOOWOOvOOincslO focsi\ocMfnoomcMcriCMONcococr\ r^u-iinco>*foooooocor^r-'>o cnoocM\DcMr~\or^ONtT>\oo\o<- r~io\or^irior^soPOooror^cM'vO _(i— l,-li— (>— ICM-Hi-).— I.— Ii— I.— ICM>— I O B 00 00 00 00 00^ 3 3 3 3 3 C O Q O O O & O O B B ^ 00 bOAi B 3 3 B 1=) Q O !3 O B 3 B Q & ^ )^ M M u o u o u O to U > U CJ M a. (u (U > 0) -H B t>. >> s B (JO O "O O •H to -O « >t >-l 3 OO to 3 u u • B ^ o to O hJ 3 I I CO * 1-1 CVJ Table 47. Dates of movements to dens and final entry of dens for black bears. 1981 - 1983. Bear Movement to Approximate Reproductive No. Sex Age Year Den Site Den Entry Status 509 F 10.5 1981 Oct. 13 Oct. 13-16 Pregnant 212 M 6.5 1981 Oct. 22 Oct. 28 mm 509 F 11.5 1982 Nov. 4 Nov. 8-18 Cubs present 523 F 3.5 1982 Oct. 25 Nov. 2 Pregnant 517 M 5.5 1982 Nov. 8 Nov. 8-18 ... 523 F 7.5 1983 Oct. 28 Nov. 5-9 No cubs 506 M 4.5 1983 Nov. 5 Nov. 9-27 515 M 4.5 1983 Oct. 5 Nov. 9-27 - Table 48. Dates of den emergence and movement from den sites, 1982-84. Bear No. Sex Age Year Approximate Movement from Den Emergence Den Site Reproductive Status 509 F 11.5 1982 Apr. 23 May 1 Cubs present 212 M 7.5 1982 Apr. 2-9 Apr. 10 ^ 509 523 F 12.5 1983 Apr. 1-6 Apr. 7 Yearlings present F 4.5 1983 Mar. 10-26 Mar. 26 No cubs 517 M 6.5 1983 Apr. 5 Apr. 18 523 F 5.5 1984 Apr. 1-3 Apr. 4 Cubs present 506 M 5.5 1984 May 1-5 Apr. 1-4 _ 515 M 5.5 1984 March 26-28 May 5-8 - Black Bear Habitat Use This phase of black bear data was not completed at the time of this report. Black bear habitat use was previously summarized (Aune et al. 1983 and 1984). Work will continue on this subject for inclusion in the final project report. Population Data. 1976-1986 During 1976-1986 at total of 69 and 70 black bears were captured and marked north and south of the Sun River, respectively (Appendix D) . A grand total of 139 bears were marked, for an average of 12.6 new bears captured each year. Table 51 presents the number of black bears trapped, recaptured, and hunter killed during 1976-1986 for the north and south study areas. ?coi?^ ^-^^"^^ ^^^^^ captured, 102 (73%) were males and 37 (27%) were females. 74 (53%) were subadults, 55 (40%) were adults, 8 (6%) were yearlings and 2 (1%) were cubs. Sex and age ratios of captured bears were only slightly different between the north and south study areas (Table 51) (Appendix E) . The mean age of black bears captured on the East Front was 5.5 years. -116- B^ in -H \o o — 1 r~. fH in o 00 I-H 00 CO CO 00 ON St sr o rv. 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B I I I ■ I I I SB < I • I I I t m H ; , , flO CN yj a- o CM x) m 00 in CM u^ . • *>in )1-» •H C 3 w (U ,£! 4J o 4J s o CO c CO J= 4-1 >-l O c c o M pt< 4J Cfl CO w c •H CO U G 3 o S >^ CJ O Pd cu 4-> c o -o — I f-H CM •-H CM in 1^ \0 VO CM CM C»^ O CM O 00 O CO CT\ m m ^o 00 CM a> 00 -* 00 «a- 00 — I \o CM O — I O CO O '-H •o- 1-H m ■— I r^ 1— I CM CM m ^ r^ \o CM CO 1 1 1 CTv • t-H 1 1 1 1 CJN CM • CM 1 1 1 1 C3^ • 1-4 o o • o 1— 1 i-H CO • CM • c^ CO • sf— ico—t-o-incM o CM •-( i-H \0 O O CM O CO VO O CM m -* in m I-H CM CM \D <■ 1^ ^ in I-H m CM CO • CO 00 00 \o Oi 00 00 1 in • • • • « • • 1 • CO r~ r- m »— 1 »* 00 1 CM CO i-H 1-4 f— i 1 I-H o o CO o m • CM m CO cu 00 i-i CO CO u 4J H < (Table 53). Using the Lincoln Index: N=Mn m : where N=total population size M=total number of individuals originally marked n=total number of individuals caught at a subsequent time m=total previously marked individuals caught at a subsequent time; N = 10(13) = 65 black bears 2 The estimated area used by these bears was determined by drawing a circle, with a radius of % the average standard home range diameter, around each capture site within the trap circuit and determining the area enclosed by these circles using a planimeter. The average standard home range diameter was derived from the standard home range diameter for male and female black bears radioinstrumented in the Deep Creek-Birck Creek study area, weighted by the number of males and females caught during the sample period in the Beaver Creek-Willow Creek area. The resulting area was 728 km^ (281 mi^) (Fig. 46). The minimum density estimate for this area was 1 bear/34.7 km^ (13.4 mi^), and the total density estimate was 1 bear/11.2 km^ (4.3 mi^). The density estimate for the Deep Creek-Birch Creek study area was derived from the composite home range of radioinstrumented black bears, modified to exclude habitat unsuitable to black bears along the eastern edge of black bear range, (Fig. 47) to determine the area, and the number of radioinstrumented and unmarked but identifiable observed bears for the total population estimate (Aune et al. 1984). The area of the composite home range was 1101 km^ (425 mi^) and the total population estimate was 39 bears for a density of 1 bear/28.2 km^ (10.9 mi ). Without excluding unsuitable habitat the composite home ranee was 1136 km^ (439 mi^). After deriving density estimates for the Beaver-Willow Creek and Deep Creek-Birch Creek area we calculated a population estimate for the entire East Front by applying the density for the Beaver-Willow Creek area to the BMUs (North Fork Sun River, South Fork Sun River, Dearborn-Elk Creek; total area 2202 km (850 mi^); N=198 bears) (Figures 32, 33 and 34) with habitat similar to that area, and applying the density for the Deep Creek-Birch Creek area to the BMUs (Badger-Two Medicine, Teton-Birch Creek, Teton- Sun River; total area=3549 km=^ (984 mi ), N=126 bears) (Figures 29, 30 and 31) with habitat similar to that area. This method yielded a total population estimate of 324 black bears for the East Front. It is most likely that the black bear density in the northern regions is somewhat higher than estimated. The total area of black bear habitat used in our analysis is probably over estimated because it is based on area calculations from grizzly bear BMUs. Data from radioed black bears indicated they probably do not extend easterly as far as grizzly bears and are more closely tied to timbered habitats along the front. Reducing the size of the total area would reduce the population estimate. At this time no other population estimate is ■125- « Captur* Sit* Figure 46. Area used for Beaver Creek-Willow Creek density estimate. -126- Figure 47. 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HO ^^ iH 0) w 'Hcnvor^ON'-immr~-i~--»<-~^-mmmmmmmmmm r-l 00 I 00 CM available for the Rocky Mountain Front. Further work is needed to validate these estimates. Black Bear Harvest Rate In 1986, 61 black bears were harvested along the Front by hunters as determined by the mandatory hunter tooth check established in 1985. (Table 54). Considering the total population estimate the harvest rate was 19% for 1986. Data from 1985 indicated a harvest of 34 black bears via the tooth check information (Table 55), for an estimated harvest rate of 11%. The average harvest rate for the last two years is 15%. Recommended black bear harvest rates range between 10-20% in North America (Erickson 1965, Poelker and Hartwell 1973, Waddell and brown 1984, Kohn 1982). Kasworm (1986) recommends a harvest rate of 10% for northwestern Montana. Considering that the density of bears in his study area is higher and the population is probably more productive than in the East Front, a higher level of harvest would not be suitable for the drier less productive black bear habitats of central Montana. An annual harvest of 61 bears at a harvest rate of 10% requires a population of 610 black bears considerably more than our current estimate of 324 black bears. A population of 610 black bears along the East Front would translate into bear densities of 1 bear/3.0 sq. mi. a density more common to areas with richer coniferous forest and better quality habitat. Harvest rates calculated for the East Front may be underestimated due to noncompliance with the mandatory tooth check regulation. It is likely that actual harvest thus presented are actually higher. Jerry Brown (pers. comm.) indicated that compliance with the reporting regulation in Montana's management region 1 was 70% in 1985 and that compliance in 1986 was improved but still below 100%. A compliance rate of 70% in 1985 would correct our 1985 harvest to 49 black bears and our 1985 harvest rate to 15% raising our two year harvest average to 17%. While a harvest of 15-19% might be acceptable as a one year perturbation, a long term harvest rate of this level could reduce the population along the East Front and will certainly affect the age structure and quantity of trophy black bears along the East Front. This level of harvest coupled with the poor bear food years of 1985 and 1986 with subsequent higher natural mortality and lower production may quickly impact the population. Recent studies suggested that the nutritional base affects cub production and survival (Jonkel and Cowen 1971, Rogers 1976, Beecham 1980, Alt 1982, Lecount 1982, and Hugie 1982) . The absence of annual production data and harvest trends from the East Front to measure the impact of increased harvest rates and drought conditions creates further concern. Data on the age and sex composition of the harvest on the East Front are also of concern. In 1985 the median age of harvested males, females and both sexes combined was 3.5 years. In 1986 the median age for each of these sex classes was 4.5 years. The sex composition of the harvest was 75% male, 25% female in 1985, and 71% male, 29% female in 1986. In 1985 the subadult: adult ratio of the harvest was 63:37 and in 1986 it was 61:39. Kasworm (1986) reported that the median age decreases and the subadult proportion of the harvest increases as hunting pressure increases on black bears. Similar findings have been reported •129- Table 54. Black bear harvest from the Rocky Mountain East Front, 1986. Hunting Bear Date District Location Sex Age Color No. 4/17 424 Ford Cr. M 10.5 Brown _ 4/26 442 S. Fk. Teton R. M 4.5 Brown — 5/6 424 Elk Cr. M 5.5 Brown _ 5/16 422 Green Cr. F 15.5 Black _ 5/16 424 Smith Cr. F 4.5 Black 405 5/17 425 Willow Cr. F 7.5 Brown 5/18 424 Beaver-Willow M 2.5 Black , , 5/18 425 Burdoff F 4.5 Brown .. 5/20 442 Green Timber Cr. M 9.5 Black 352 5/21 424 Elk Cr. M 6.5 Black 478 5/22 422 Elk Cr. M 4.5 Brown 353 5/24 442 Lynx Cr. M 10.5 Black 5/25 424 Elk Cr. M 9.5 Brown 354 5/26 422 Sawmill Cr. M 4.5 Black 495 6/3 442 Rierdon Gulch F 4.5 Black 6/12 424 Beaver Cr. M 1.5 Black ■IK 6/14 442 N. Fk. Sun R. M 2.5 Black ^ 7/5 442 Big George F 16.5 Brown _ 7/20 442 Big George M 4.5 Black _ " 7/26 442 - M 2.5 Black .. 8/2 424 Fairview Cr. F 7.5 Black 417 8/10 441 Birch Cr. M 1.5 Black 8/22 441 Jones Cr. F 2.5 Black , „ 9/1 424 Fairview Cr. M 1.5 Black .^ 9/2 406 Birch Cr. M 2.5 Black _ 9/3 406 Teton R. M 2.5 Black ^ 9/8 406 Teton R. F 9.5 Black _ 9/13 424 S. Fk. Sun R. M 4.5 Brown _ 9/13 441 E. Fk. Teton R. M 4.5 Brown _ 9/20 425 Rose Cr. M 5.5 _ 9/20 425 N. Fk. Barrs Cr. M 4.5 Brown „„ 9/20 442 Sawmill Flats F 1.5 Black _ 9/21 442 Beaver Cr. M 10.5 Balck 427 9/25 422 Blubber Cr. M 15.5 Black 202 9/27 422 Elk Cr. F 6.5 Blond 345 9/28 422 Cunniff Basin M 4.5 Brown 337 9/28 441 Dupuyer Cr. F 8.5 Black 531 10/1 442 Ear Mtn. M 7.5 Brown 10/3 450 Teton R. M 7.5 Black _ 10/4 441 S. Fk. Dupuyer Cr. M 2.5 Brown „„ 10/4 404 Beartooth F 13.5 Black 105 10/5 442 Teton R. F 8.5 Brown 10/5 442 Deep Cr. M 5.5 Black ■»• 10/6 441 Scoff in Cr. M 2.5 Black «. -130- I Table 54. Black bear harvest from the Rocky Mountain East Front, 1986. Hunting Bear Date District Location Sex Age Color No. 10/6 442 Deep Cr. F 1.5 Brown 10/7 442 Deep Cr. M 4.5 Black 10/7 442 Ear Mtn. M 2.5 Brown 10/8 415 East Glacier M 2.5 Black 458 10/11 422 Green Cr. M 4.5 Brown 10/11 450 - M 2.5 Black 10/11 450 Teton R. F 2.5 Black 10/21 441 Crazy Cr. M 4.5 Black 10/22 422 Elk Cr. M 2.5 Black 11/2 442 Arsenic Cr. F 3.5 Black 11/23 441 Dupuyer Cr. M 3.5 Brown 6/8 415 Two Medicine R. M 12.5 Black 10/11 442 Little Willow Cr • M 2.5 Black 9/26 424 Wood Lake M 4.5 Black 4/17 441 Cow Cr. M 6.5 Brown 4/20 441 Teton M 7.5 Black 5/6 415 S. Fk. Two Medicine R. F 4.5 Brown - 8072/2 -131- Table 55. Black bear harvest from the Rocky Mountain East Front, 1985. Hunting Bear Date District Location Sex Age Color No. 5/6 424 Smith Creek M 7.5 Black _ 5/8 424 Ford Creek M 3.5 Brown 5/11 424 Smith Creek M 15.5 Brown _ 5/15 422 Elk-Blubber Cr. M 5.5 Black 535 5/15 441 Scoff in Cr. M 6.5 Black 5/16 422 Blubber Cr. M ? Black 5/18 442 Rierdon Gulch M 7.5 Black 517 5/20 442 Rierdon Gulch M 6.5 Black 5/23 424 Ford Creek F 15.5 Black _ 5/25 428 Lange Creek M 2.5 Black 5/25 442 Arsenic Cr. M 1.5 Brown 5/2b 424 Bear Gulch M 7.5 Brown 5/27 424 Fairview Creek; M 7.5 Brown 492 5/28 442 Hannon Gulch M 1.5 Black 6/1 ^ 1 f\ 425 Sun River Game Range F 21.5 Cinnamon 380 6/2 442 S. Fk. Teton River M 3.5 Black 6/4 442 Waldron Creek M 2.5 Brown 6/6 442 Ear Mountain M 2.5 Black _ 6/6 442 Ear Mountain F 3.5 Brown 6/15 441 N. Fk. Teton River F 2.5 Brown 6/15 442 N. Fk. Sun River M 4.5 Brown 7/? 442 Moose Creek M 3.5 Blonde 330 8/11 441 Jones Creek M 6.5 Black 515 9/6 422 Falls Creek M 3.5 Black 370 9/25 406 Teton River M 3.5 Brown 9/25 442 Little Willow Cr. M ? Black 10/27 424 Lime Gulch M 1.5 Brown 10/29 442 Stovepipe Cr. F 12.5 Brown 10/29 422 Joslln Basin F 2.5 Black 362 10/31 424 Smith Creek F 1.5 Black 10/31 424 Willow Creek M 1.5 Brown 11/3 422 Falls Creek M 4.5 Black 11/5 442 Blacktail Creek M 1.5 Brown 11/6 428 Bighead Creek F 3.5 Black 400 8072/2 -132- elsewhere in North America (Beecham (1980, Hugie 1982, Kohn 1982, Modafferi 1982, Woddell and Brown 1984). Although we do not have data from enough years for the East Front to make these comparisons, the median age and subadult proportion of the harvest are similar to those reported by Kasworm (1986) as being cause for concern. Management guidelines for black bears in MDFWP Administrative Region 1 call for 1) median age of harvested females 1-2 years above age of first production, 2) female proportion of the total harvest should not exceed 40%, 3) subadult proportion of the total harvest should not exceed 50%, and 4) the harvest rate should be approximately 10%. Our data for the East Front indicates that the age at first reproduction is 5 years or greater, female proportion of the harvest is 28%, subadult proportion of the harvest is 61%, and the harvest rate is 15-19% over the past two years. These data show that the harvest on the East Front exceeded three of the four criterion. Actions should be initiated to bring these parameters within responsible management guidelines. It is our recommendation that hunter harvest be reduced to 10% for the Rocky Mountain Front region. This could be accomplished by restricting season length, permit hunting, quotas, or redistribution of hunter pressure. Hunting harvest may be related to accessibility of an area by vehicle (Hugie 1982, Lecount 1982, and Manville 1983). Although data are not available for the front area specifically, observations seem to support that much of our harvest comes from drainages and areas accessible with vehicles (Table 56). These do not comprise whole hunting districts but most generally portions of districts. A significant portion of the black bear habitat is within remote wilderness areas. In these portions harvest rates are generally low. Some redistribution of hunting pressure is possible but it would not likely reduce hunting harvest appreciably. Harvest rates by hunting district could not be calculated. However, further work could produce some data by hunting district groups and further monitoring of harvest could provide hunting harvest trends. Mandatory tooth collection should be continued along the front because this may be the only data base from which to base management decisions. Table 56. Black Front bear , 1985 harvest by hunting district for and 1986. the Rocky Mountain East Year 404 406 415 422 Hunting District 424 425 428 441 442 450 Tota 1985 0 1986 1 TOTAL 1 1 3 4 0 3 3 5 8 13 9 1 2 11 4 0 20 5 2 3 10 13 13 18 31 0 34 3 61 3 95 Some specific problem areas may exist on the Rocky Mountain Front. Heavy hunter pressure is being experienced in local areas such as Elk-Blubber Creek, Ear Mtn. WMA, and Jones Creek. These areas are popular to the sportsman and could be mortality sumps that are maintained only by their proximity to remote and wilderness areas. Hunting district 415 reports only 3 black bears harvested in two years. This is productive black bear habitat adjacent to the Blackfoot -133- Indian Reservation. Black bears harvested by the tribal members may not be reported to the Montana Dept. of Fish, Wildlife, and Parks. The absence of such information is likely to make season setting for this district difficult. Data from grizzly and black bear studies demonstrates the interdependence of foothill and front country to the interior mountains in providing a complete habitat for bears. This interdependence means that management of black bears in H.D. 415 is related to management of adjacent areas in the Blackfoot Reservation. The most likely options to appreciably reduce harvest rate of black bears are restricting season length, permit hunting, or quotas. Season length adjustments are not likely to reduce recreation opportunity as much as the other two. A split season from April 15 to May 31 and Oct. 1 to Nov. 30 could result in a harvest rate of 9% if there is a direct correlation with bears killed and hunter effort over time (i.e. a reduction of 37 harvested bears based on data from Table 57). However it is likely that restrictions in season length will result in greater hunter effort during a shorter time frame rather than a reduction in the harvest. If season restrictions are imposed, monitoring of harvest rate should be initiated to evaluate whether this rate is affected. Table 57. Monthly black bear harvest by hunting district for the Rocky Mountain East Front, 1985-1986. Hunting District Month 404 406 415 422 424 425 428 441 442 450 Total April 0 0 0 0 1 0 0 2 1 0 4 May 0 0 1 5 11 2 1 1 6 0 27 June 0 0 1 0 1 1 0 1 7 0 11 July 0 0 0 0 0 0 0 0 4 0 4 August 0 0 0 0 1 0 0 3 0 0 4 Sept. 0 4 0 4 3 2 0 2 3 0 18 Oct. 1 0 1 3 3 0 0 3 8 3 22 Nov. 0 0 0 1 0 0 1 1 2 0 5 Total 1 4 3 13 20 5 2 13 31 3 95 It is unlikely that black bear management in Montana will remain simple. More sophisticated forms of data will be necessary to make management decisions. The absence of trend data on harvest rates, production data, and limited population data coupled with complex demands of the users of this wildlife resource can only increase the potential for problems with management in the near future. Without adequate biological information bears, cats and other large predatory/scavenger wildlife species are susceptible to overharvest (Beecham 1983, Bunnell and Tait 1981, Hemker 1984 and Harris 1984). These species require different management philosophies and harvest programs than large herbivores. High mobility, low density, complex prey relationships, and propensity to conflict with humans in fact or fiction make large carnivorous species more sensitive to slight but increased selection pressures by sportsmen. As such, management has to be correspondingly more sensitive to changes in the biological parameters of the population. -134- MANAGEMENT RECOMMENDATIONS Management Guidelines Rapid distributional recession and declines in grizzly bear populations occurring with the development of increased human activity has been well documented in Europe and North America (Martlnka 1982, US Fish and Wildlife Service 1981, Roben 1980, Cowan 1972, Mysterud 1980, Buchalczyk 1980, Markov 1980, Roth 1976, Elgmork 1978, Grachev 1976, Kaal 1976, Vereschagin 1976, Pearson 1975, Curry-Llndahl 1972, Stebler 1972, Zunino and Herrero 1971, Guilday 1968, Buss 1956 and Storer and Trevis 1955). Human activities within grizzly bear range will continue to have effects, however subtle, on grizzly bears. Management guidelines developed by the Interagency Wildlife Monitoring and Evaluation Program were developed as a direct result of grizzly bear monitoring conducted on the east front (Appendix F) . If followed, these guidelines will mitigate but not eliminate detrimental influences of human activities on grizzly bears and grizzly bear habitat. Cumulative Effects Recent studies in North America have expressed concerns regarding Increasing human access and activities within grizzly bear habitat. The influences of timber harvest, livestock grazing, boneyards and dumps, recreation, sport hunting, road access, mining, subdivision, and hydrocarbon exploitation have been discussed (Craighead 1979, 1980, Craighead and Craighead 1967, 1971, 1973, 1974; Knight et al. 1975, 1976, 1977, 1978, 1980, 1980a, 1981; Chester 1976, Jonkel and Servheen 1977, Jonkel 1976, 1977, 1978, 1980; Harding and Nagy 1980; Schallenberger and Jonkel 1980, Knight and Judd 1980, Blanchard 1978, 1980; Servheen 1981, Pearson 1975, Reynolds and Hechtel 1980, Nagy and Russell 1978, Russell et al. 1978, Hamer et al. 1977, Mundy and Flook 1973). Each activity contributes an additive stress to grizzly bear populations. It is recommended that responsible agencies continue to develop the ongoing cumulative effects model to measure impacts of human activities. Modeling results should be biologically validated using scientific research techniques and the existing grizzly bear data base. Application of the model should occur only after complete development and validation are completed. The model should be continually refined as knowledge and data indicate a need for revision and refinement. Such a project has widespread applicability to all wildlife species concerned. Research Studies The relationship of grizzly bears to all types of human activities as well as oil and gas development must be understood. Monitoring programs should be further directed and focused toward filling important gaps in the data base. A summary of existing data is needed to indicate where these gaps exist. Analysis of habitat preference, denning habits, distribution, food habits, movement and home range data should be continued. Intensive efforts to gather data pertaining to livestock/bear relationships, population estimation, oil and gas development impacts, the role of sport hunting, the effects of animal depredation control programs, and the interaction of black and grizzly bears deserve further investigation. Field emphasis should be directed toward securing baseline data in the south half of the Badger-Two Medicine BAU, the area south of the Sun River, and the remote backcountry areas. -135- Other Management recommendations were previously presented (Aune et al. (1981, 1982, 1983, 1984, 1985, and 1986)). It is recommended that work continue on the Montana Department of Fish, Wildlife, and Parks zoned management plan for the East Front. Regional Management Plans are essential to proper direction and devising management to achieve specific goals. Efforts should be made to coordinate regional plans with existing interagency programs and recovery objectives for grizzly bears. Mortality and population trend monitoring programs should be outlined in the management plan so that program revisions and refinements can be made. 8072/2 -136- LITERATURE CITED Alt, G.L. 1982. Reproductive biology of Pensylvania ' s black bear. Pa. Game News. 53(2): 9- 15 Amstrup, S.C. and J. Beecham. 1976. Activity patterns of radio-collared black bears in Idaho. J. Wildl. Manage. 40(2) :340-348. Andrews, R.V. 1979. The physiology of crowding. Comp. Biochem. Phiol. 63A:l-6. Archibald, W.R., R. Ellis, A.H. Hamilton. 1986. Responses of Grizzly Bears to Logging Truck Traffic in the Kimsquit River Valley British Columbia. Presented to the International Bear Conf., Williamsburg Virginia, (In Press) . Aune, K., Bob Brannon. 1986. Rocky Mountain Front Grizzly Bear Monitoring and Investigation. Mont. Dept. Fish, Wildlife and Parks. Helena. 195 pp. 1985. Rocky Mountain Front Grizzly Bear Monitoring and Investigation. Mont. Dept. Fish, Wildlife and Parks. Helena. 138 pp. and T. Stivers. 1981. Rocky Mountain Front grizzly bear monitoring and investigation. Mont. Dept, Fish, Wildl, & Parks. Helena. 50pp ^^^ • 1982. Rocky Mountain Front grizzly bear monitoring and investigation. Mont. Dept. Fish, Wild. & Parks. Helena. 143pp. and . Stivers. 1983. Rocky Mountain Front grizzly bear monitoring and investigation. Mont. Dept. Fish, Wildl. and Parks. Helena. 180 pp. and , and M. Madel. 1984. Rocky Mountain Front grizzly bear monitoring and investigation. Mont. Dept. Fish, Wildl. and Parks. Helena. 238 pp. and Stivers. 1985. Ecological Studies of the Grizzly Bear in the Pine Butte Preserve. Mont. Dept. Fish, Wildl. and Parks. Helena. 154 pp. Beecham, J.J. 1980. Some population characteristics of two black bear populations in Idaho. Int. Conf. Bear Res. and Manage. 3:201-204. Beecham, J.J. 1983. Population characteristics of black bears in west central Idaho. J. Wildl. Manage. 47(2) :405-412 Blanchard, B. 1978. 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Publ. N.S. No. 23. pp. 74-80. Dood, A.R., R.D. Brannon, and R.D. Mace, 1986. Final Programmatic Environmental Impact Statement, The grizzly bear in northwestern Montana, Mont. Dept. of Fish, Wildlife, and Parks, Helena, MT. 279 pp. Dupuyer Centennial Committee. 1977. By gone days and modern ways. Griggs Printing and Publishing. Havre, MT. 388pp. Elgmork, L. 1978. Human impact on a bear population (Ursus arcots L.) England Biol. Conserv. No. 13:81-103. Erickson, A.W. 1965. The black bear in Alaska. Alaska Dept. of Fish and Game. Juneau. 19 pp. Erickson, G. L. 1972. The ecology of Rocky Mountain bighorn sheep in the Sun River area of Montana with special reference to summer food habits and range movements. M.S. thesis, Mont. St. Univ., Bozeman. 50pp. Frisina, M. R. 1974. Ecology of bighorn sheep in the Sun River area of Montana during fall and spring. M.S. thesis, Mont. St. Univ., Bozeman. 68pp. Garshelis, D.L. and M.R. Pelton. 1980. 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CO •H rH •H O Cd ^ 00 CO •H Cd 00 CO C rH Cd B § u ex u t» o O -H -H cd cd >..i o •n Vi Ij iM CO x) cd cd •H ,H ,H C rH cd 3 3 S •H CJ O O O y -H -H -H c ^ U U U M u u u u c (JOO & !=) to cd CO U -H •H rH O 3 •H 73 X) cu cd cd c a cd cd •H -H >^ u (a > CO 01 y 4-1 (U • XI ft-H •H ft Vj CO CO -H - Cd > Cd Cd B 4J cd cd y cu -H Cd cd 3 M VJ 4-) 0) oj cd rH rH H cd > > > Cd cd o C -H > Cd -H Cd Ai c y 0) 0) > > > ou-iooooomooooocn-o-r^ vpvovor~.ooor-ieMcosi--*»a-«* 0^o^0^0^o^0^a^00000000 ■^t-Ji-sj-^sj-st-si-iriminioiriiniriio cd 4-) Cd y c 3 Cd C Cd y cd •H > ^4 -rl ^ 4J Cd CO Cd X! Cd 6 C rH ftrH 3 Cd 0) rH O 3 M y 73 cdcdcdcdcdcdcdcdcd y y •rl -H > > y o o o o o •H -rl -rl -H -H -H >>>>>> CO rH 3 >^ B Xi 0) ftXl O Cd B cu XI •H y y o >-^ cd U CO cu ^ 4J h ft o cd <4H ^ 00 00 N 0) -H -H -H !>< N N N Cd U O H oomoooomooomoooo iDvOvOvOt^OOOOOsOrH— ic>)COh Teton River Orange /Red (metal) Brown Hunter-kill (>I3/19. 5/12/78 211 M 19 Teton River Yellow/Orange Black Relocated to Blackleaf . * (metal) 8/21/80. b/OdllS 212 M ih Blackleaf Blue /Red Black Recaptured 9/25/80 (metal) & 6/23/81 & radioed. Recaptured 5/24/82. * Hunter-kill 7/11/82. 6/13/78 202 M 15 Elk Cr. Orange /Blue (metal) Brown Recaptured 5/2/84 % Elk Cr. Hunter-kill 6/U/l^ 205 M Adult Elk Cr. Orange /Red (metal) Black 9/25/86. Unknown . 5/20/79 288 M 17 Blackleaf Green/Red Brown Recaptured 5/10/80 (metal) & 6/29/82 & radioed. Radio off Sept. 1982. * = age at death -180- Appendix D. Black bears captured on the East Front, 1976-1986, (continued). DATE OF CAPTURE NO. SEX 5/28/79 6/09/79 6/09/79 5/19/80 5/21/80 5/28/80 5/30/80 6/07/80 6/09/80 5/20/81 5/23/81 5/27/81 5/02/82 5/17/82 5/17/82 514 M AGE (1986) LOCATION 5/22/82 6/19/82 6/24/82 255 F 10 Teton River 115 M 14 Teton River 294 M 9%* Teton River 329 M 5J5* Blackleaf 223 M 9 Blackleaf 538 M 5J5* Blackleaf 505 M 8 Blackleaf 542 M 5^5* Blackleaf 509 F 15 Blackleaf 545 F 8 Blackleaf 546 F 8 Blackleaf 516 M 8 Blackleaf 539 M 4% Teton River 513 M 6 Teton River Ih Teton River 531 F 8 Dupuyer Cr. 523 F 9 Teton River 517 M 7's* Teton River 7/12/82 533 F 10% Badger Cr. EAR TAG (TYPE) COLOR FATE Orange/Silver Brown (metal) Yellow/Green Brown (metal) Green/Orange Black (metal) Yellow/Red Black (metal) Blue Brown (rototag) Blue Brown (rototag) Red Black (rototag) Blue Black (rototag) Red Black (rototag) Blue Black (rototag) Blue Brown (rototag) Red Brown (rototag) Blue Brown (rototag) Red Brown (rototag) Red Brown (rototag) Blue Black (rototag) Red Black (rototag) Red Black (rototag) Blue Brown (rototag) Recaptured 5/16/82. Unknown . Recaptured 5/23/82. Hunter-kill 5/23/82. Hunter-kill 8/6/80 (a Cave Mtn. Unknown. Hunter-kill June 83 @ Ford Cr. Recaptured 9/1/80. Hunter-kill 10/28/82 @ Green Timber Gulch. Recaptured 5/14/81 & radioed; observed 8/22/84. Recaptured 5/21/81. Unknown . Unknown . Hunter-kill 11/3/83 Patricks Basin. Recaptured 6/19/83, 5/17/84 at Sun River Game Range. Recaptured 6/26/82. Hunter-kill 10/2/82 @ Jones Cr. Hunter kill 9/28/86. Radioed until 5/25/84 when collar was cast. Radioed. Recaptured May, 1983, collar dead. Hunter-kill 5/18/85 @ Reirdon Gulch. Hunter-kill 10/19/83 (3 Badger Cr. age at death -181- Appendix D. Black bears captured on the East Front, 1976-1986, (continued). DATE OF AGE CAPTURE NO. SEX (1986) LOCATION 4/30/83 530 M 354 4/30/83 535 M 365 5/18/83 536 M 5/19/83 506 M 5/24/83 515 M Blubber Cr. 1 5/27/83 6/11/83 6/12/83 6/13/83 6/16/83 6/17/83 6/18/83 6/20/83 6/21/83 6/25/83 6/25/83 6/27/83 6/27/83 7/12/83 7/12/83 537 M 532 M 525 F 534 M 478 M 479 F 520 M 507 M 477/ F 409 491 F 492 M 494 F 476 M 520 M 547 M 8/05/83 401/ F 426 11 , * eh* 4%* , * 5h 1 6 6 4 5 4 13 5 Ih* 3 6 6 Blubber Cr. Blubber Cr. Fine Butte Rinkers Cr. Blubber Cr. Willow Cr. Blubber Cr. Sun River Game Range Sun River Game Range Beaver Cr. Blubber Cr. Blubber Cr. Willow Cr. Beaver Cr. Beaver Cr. Rose Cr. Willow Cr. N. Fk. Badger Cr, Whiterock S. Fk. Teton EAR TAG (TYPE) COLOR FATE Blue /Green (rototag) Blue/Green (rototag) Blue (rototag) Red (rototag) Red (rototag) Blue (rototag) Blue (rototag) Red (rototag) Blue (rototag) Green (rototag) Green (rototag) Red (rototag) Red (rototag) Green (rototag) Green (rototag) Green (rototag) Green (rototag) Green (rototag) Red (rototag) Blue (rototag) Green (rototag) Brown Black Black Black Black Recaptured 5/27/83, 5/4/84, renumbered 354 on 6/3/84, recaptured 5/17/86. Hunter-kill 5/25/86. Recaptured 6/17/83, renumbered 365 on 5/12/i Hunter-kill 5/15/85. Recaptured 5/27/83 & 6/15/83, 5/12/84. ■ Radioed. Hunter-kill SeA 1984 @ Jones Creek. Radioed until 5/11/84, _ collar dead. Hunter-killB 8/11/85 (a Jones Cr. ■ Unknown . I I I 1 I Black Black Black Black Black Black Black Black Brown Black Brown Black Black Unknown. Cinnamon Recaptured 5/26/86. Black Recaptured 6/4/84. Hunter-kill September 1984 @ Badger Cr. Black Nuisance bear captured @ Circle 8. Nuisance bear recaptured 8/30/86, renumbered 426. Hunter-kill 5/21/84 @ Ford Cr. Recaptured 5/25/86. Recaptured 6/27/83, 5/11/84. Probably hunter killed 5/21/86, tatoo id.? Unknown. Unknown . Recaptured 6/22/83, 5/17/84. Recaptured 5/21/86 & renumbered 409. Unknown . Hunter-kill 5/27/85 @ Farview Cr. Unknown . Two black bears * = age at death inadvertantly #'d the same - one is cinnamon and one is black. -182- Appendix D. B lack bears c aptured on the East Front, 1976- -86, (continued). DATE OF AGE EAR TAG CAPTURE NO. SEX (1986) LOCATION (TYPE) COLOR FATE 5/02/84 327/ M 12 Willow Cr. Green Brown Recaptured 5/23/84, 418 * (rototag) renumbered 418 on 6/27/86 5/05/84 352 M 9 Beaver Cr. Green (rototag) Black Recaptured 5/12/84 at Middle Fk. Beaver Ck. Hunter-kill 5/20/86. 5/07/84 455 M 4 Blubber Cr. Green Cinnamon Recaptured 5/28/84 * (rototag) Goss Ck. 5/08/84 353 M 4 Beaver Cr. Green Cinnamon Hunter-kill 5/22/86. (rototag) 5/08/84 475 M 9 Elk Cr. Green (rototag) Black Recaptured 5/11/84 at Sawmill Pass. 5/10/84 364 F 4 Sun River Game Range Green (rototag) Brown Unknown . 5/10/84 339 M 11 Ford Cr. Green (rototag) Brown Unknown . 5/10/84 344 M 3 Beaver Cr. Green (rototag) Blonde Unknown . 5/12/84 332 M 4 Blubber Cr. Green Cinnamoi? Recaptured 5/18/84 at (rototag) Sawmill Pass and 6/10/84 at Blubber Cr. 5/13/84 375 M 16 Sun River Game Range Green (rototag) Black Unknown. 5/14/84 331 F 7 * Willow Cr. Green (rototag) Brown Recaptured 5/18/84 & 5/16/86. 5/18/84 495 M 4 Elk Cr. Green (rototag) Black Hunter-kill 5/26/86. 5/19/84 388 M 2?5 Smith Cr. Green (rototag) Brown Hunter-kill in October 1984 @ Elk Creek. 5/22/84 380 F 21%* Shed Cr. Green (rototag) Cinnamon Hunter-kill 6/1/85 @ Sun River Game Range. 5/22/84 387 M 3 Shed Cr. Green (rototag) Black Unknown. 5/23/84 389 F 4 * Beaver Cr. Green (rototag) Black Unknown. 5/26/84 393 M 9h Elk Cr. Green (rototag) Black Hunter-kill August 1984 @ Elk Cr. 6/02/84 383 M 5 . * Blubber Cr. Green (rototag) Black Recaptured 6/4/84 at Sawmill Cr. and 6/13/84 at Goss Cr. Hunter-kill 10/15/86 6/03/84 399 M 4*5 Elk Cr. Green (rototag) Brown Hunter-kill 10/19/84 @ Bighorn Lake. 6/04/84 318 M 4 Gross Cr. Green (rototag) Black Unknown . 6/05/84 360 M 4 Hyde Cr. Green (rototag) Black Unknown. 6/07/84 356 F 4 Mettler Coulee Green (rototag) Black Recaptured 5/29/86. 6/09/84 345 F 6 Cyanide Cr. Green (rototag) Blonde Hunter-kill 9/27/86. * = age at death -183- Appendix D. Black bears captured on the East Front, 1976- 1 -86, (continued). DATE OF AGE EAR TAG 1 CAPTURE NO. SEX (1986) LOCATION (TYPE) COLOR FATE 6/11/84 336 F 10 Mettler Coulee Green (rototag) Black Unknown. ■ 6/19/84 322 M 7 Mettler Coulee Green Cinnamon Unknown. (rototag) 6/19/84 386 F 4 Hyde Cr. Green (rototag) Black Unknown . ^ 6/Ul^h 349 M 15 Hyde Cr. Green (rototag) Black Unknown . ■ 6/25/84 348 M 4 Box Cr. Green (rototag) Black Unknown. eiisiu 397 M 11 Mettler Coulee Green (rototag) Black Unknown . I 6/28/84 330 M 3J5* W. Fk. Sun River Green (rototag) Blonde Recaptured 7/5/84. Hunter-kill July 1985 1 (3 Moose Cr. ■ 7/01/84 400 F 3J5* S. Fk. Sun River Green (rototag) Black Hunter-kill 11/6/85 @ Bighead Cr. ■ 7/03/84 390 M 14 . * W. Fk. Sun River Green (rototag) Brown Recaptured 6/23/86 & | 6/25/86. ^lieiu 376 M 2J5 Simms Green (rototag) Black Relocated to SRGR. mm Hunter-kill 9/11/84 I in Sun River Canyon. 10/07/84 340 M 4 Smith Cr. Green (rototag) Cinnamon Relocated to Beartooth Game Range. 1 5/14/85 362 F 2% Poplar Cr. Green (rototag) Brown Hunter-kill 10/29/85 ■ @ Joslin Basin. 5/19/85 377 M 10 ■k Cuniff Cr. Green (rototag) Black Recaptured 5/16/85 0 ■ Cuniff Cr. and 5/26/85 | % Big Skunk Cr. 5/19/85 337 M 4 Cuniff Cr. Green (rototag) Brown Hunter-kill 9lUlS(>. m 5/19/85 367 M 4 Cuniff Cr. Green (rototag) Brown Unknown. 5/25/85 370 M 3%* Cuniff Cr. Green (rototag) Black Hunter-kill 9/6/85 @ 1 Falls Cr. ■ 5/28/85 334 F 14 Cuniff Cr. Green (rototag) Brown Unknown . 5/29/85 351 M 9 Cuniff Cr. Green (rototag) Black Unknown. | 6/11/85 304 M 10 Moudess Cr. Green (rototag) Brown Recaptured 6/18/85 @ m Moudess Cr. I 6/20/85 303 M 9 Dearborn River Green (rototag) Brown Unknown . 6/21/85 309 M 8 Dearborn River Green (rototag) Black Recaptured 5/23/86 @ ■ Smith Cr. ■ 6/23/85 311 M 5 Moudess Cr. Green (rototag) Black Recaptured 5/17/86 % Smith Cr. ■ 5/15/86 407 M 3J5 Smith Cr. Green (rototag) Brown Unknown . | 5/16/86 403 M 6J5 Willow Cr. Green (rototag) Black Unknown. b * = age at death -184- Appendix D. Black bears c aptured on the East Front, 1976- -86, (continued). DATE OF AGE EAR TAG CAPTURE NO. SEX (1986) LOCATION (TYPE) COLOR FATE 5/16/86 405 F 4^* Smith Cr. Green (rototag) Black Hunter-kill 5/16/86. 5/18/86 459 M hh Badger Cr. Green (rototag) Brown Recaptured 5/23/86, 6/2/86. 5/19/86 406 M 3J5 Smith Cr . Green (rototag) Brown Unknown. 5/20/86 408 M 4% Willow Cr. Green (rototag) Brown Unknown . 5/21/86 404 F II5 Ford Cr. Green (rototag) Blonde Unknown . 5/21/86 473 M 4J2 Badger Cr. Green (rototag) Brown Recaptured 6/1/86. 5/24/86 413 M ih Willow Cr. Green (rototag) Black Unknown. 5/24/86 414 M ih Willow Cr. Green (rototag) Brown Unknown. 5/25/86 458 M ih Badger Cr. Green (rototag) Black Hunter-kill 10/8/86. 5/26/86 415 M \h Ford Cr. Green (rototag) Brown Unknown . 5ini%(> 416 M 3h Petty Cr. Green (rototag) Brown Unknown. 5/28/86 457 F 12% Badger Cr. Green (rototag) Black Unknown . 5/29/86 461 M 6% Badger Cr. Green (rototag) Black Unknown. 6/12/86 472 M 3% Badger Cr. Green (rototag) Black Unknown. 6/17/86 468 M 3*2 Muskrat Cr. Green (rototag) Brown Unknown. 6/19/86 462 M Sub- Adult Badger Cr. Green (rototag) Brown Unknown . 6/23/86 417 F 7% Fairview Cr. Green (rototag) Black Hunter-kill 8/2/86. 6/23/86 471 F 9% Kip Cr. Green (rototag) Black Unknown. 6/28/86 469 M (>h Kip Cr. Green (rototag) Brown Unknown . dll^/Sd 474 M 3h Muskrat Cr. Green (rototag) Brown Unknown 6/29/86 463 M 9h Crucifixion Cr. Green (rototag) Black Unknown. 7/10/86 482 F 3% Badger Cr. Green (rototag) Brown Unknown. 8/30/86 102 M 3% Teton River Yellow Brown Relocated to Whiterock 8/30/86 103 F Cub Teton River (rototag) Yellow Cinn. Pass. Relocated to Whiterock 8/30/86 104 M Cub Teton River (rototag) Yellow (rototag) Black Pass. Relocated to Whiterock Pass. * = ag e at death -185- Appendix D. Black bears captured on the East Front, 1976-86, (continued). DATE OF AGE CAPTURE NO. SEX (1986) LOCATION 9/6/86 437 M 10% 9/7/86 428 F 1655 9/10/86 427 M 835 9/11/86 105 F ISJs* 9/12/86 434 M hh Windfall Cr. Lange Cr. Windfall Cr. Sun River Windfall Cr. EAR TAG (TYPE) Green (rototag) Green (rototag) Green (rototag) Yellow (rototag) Green (rototag) COLOR FATE Brown Recaptured 9/9/86 Hunter-kill 9/21/86. Black Unknown. Brown Unknown . Black Hunter-kill 10/4/86. Brown Unknown. 8072/2 * = age at death -186- Appendix E. Black bears captured, and marked black bears killed by hunters each year for study areas north and south of the Sun River, 1976-1986. Year Area # Bear Captured # Marked Bears Hunter- Killed Tot. M F AD SA YR C Tot. M F AD SA YR ~C 1976 North 5 3 2 4 1 0 0 0 0 0 0 0 0 0 South - - - — — — _ _ _ .. 1977 North 11 9 2 4 7 0 0 0 0 0 0 0 0 0 South - - — — — _ _ _ _ _ 1978 North 3 3 0 2 1 0 0 0 0 0 0 0 0 0 South 2 2 0 2 0 0 0 0 0 0 0 0 0 0 1979 North 4 3 1 3 1 0 0 1 1 0 1 0 0 0 South - - - — — — _ — — _ 1980 North 6 5 1 2 4 0 0 3 3 0 3 0 0 0 South - - - — — _ mm -m mm . 1981 North 3 1 2 0 3 0 0 0 0 0 0 0 0 0 South - - — — _ _ — _ _ _^ 1982 North 7 4 3 2 5 0 0 4 4 0 3 1 0 0 South - - - — — _ » _ _ _ ^ 1983 North 5 4 1 1 4 0 0 3 2 1 2 1 0 0 South 16 11 5 5 8 3 0 0 0 0 0 0 0 0 1984 North 8 5 3 4 4 0 0 2 2 0 2 0 0 0 South 26 20 6 9 15 2 0 5 5 0 2 3 0 0 1985 North - - - - - — — 2 2 _ 2 0 0 0 South 11 9 2 6 5 0 0 7 4 3 2 5 0 0 1986 North 20 13 7 11 7 0 2 3 2 1 2 1 0 0 South 23 16 7 16 5 2 0 12 8 4 8 4 0 0 Total North 72 50 22 33 37 0 2 18 16 2 15 3 0 0 South 78 58 20 38 33 7 0 24 17 7 12 12 0 0 Total 150 108 42 71 70 7 2 42 33 9 26 15 0 0 8072/2 -187- Appendix F. Grizzly bear management guidelines. East Slope, Rocky Mountain Front. (Excerpted from Interagency Rocky Mountain Front Management Guidelines, 1984) Introduction The Interagency Rocky Mountain Front Wildlife Monitoring/Evaluation Program was initiated in 1980. A principal goal of this program was to sponsor study efforts; whereby wildlife management guidelines, based on sound scientific findings, could be developed to aid land managers in their planning of human activities along the Rocky Mountain Front. The original charter for this program specified that management guidelines were to be considered "interim" until five years of study had been incorporated into them. However, the guidelines developed thus far are currently being used as firm guidance by the involved agencies. Further, at the end of this five year period these guidelines should not be locked in concrete by the term "final". It is highly likely that studies will continue and additional findings will dictate new or revised guidelines. Therefore, these two terms will not be used and the management guideline development process and associated document are to be considered part of a dynamic planning process subject to periodic review and modification as additional study findings become available and as long as the need for them is present. In the event that on-going monitoring results in the need for a new guideline or the modification of an existing guideline, it can be submitted at anytime by the procedures described and on the form given on the last two pages of this document . The following management guidelines are based on the best information currently available. They are a result of current or recently completed studies on selected wildlife species. Field investigators conducting the studies have completed extensive literature reviews on the various species considered. The guidelines which have been formulated and presented in this document are not only the result of study findings and literature review, but incorporate the professional judgement of the technical personnel involved. Objective The need for management guidelines is predicated on management concerns involving the effects of existing and proposed land uses and human activities upon various wildlife species and their habitat. The objective of the development and application of management guidelines is to avoid or minimize the following effects of human related activities which may adversely impact some or all of the selected wildlife species being considered: A. Physical destruction of important wildlife habitat components. B. Human disturbance that would displace various wildlife species from important seasonal use areas. C. Increased direct human caused mortality. D. Increased stress due to higher human activity levels. -188- E. Direct mortality or physical impairment resulting from environmental (chemical) contaminates . F. Increased wildlife/human interaction resulting from habitat intrusion or displacement. Management Guidelines Management guidelines provide coordination measures designed to avoid or minimize the potential conflicts previously identified between human related activities and wildlife. Although many of the guidelines are applicable to a variety of human activities, some of them are specific to a single activity. Oil and gas exploration and development has received special emphasis due to the relatively high level of activity in recent years. As a result, some of the guidelines apply specifically to that activity. Approved management guidelines will be included in permits, contracts or other formal authorizations for human activities as applicable. Omissions or modifications of applicable guidelines in such authorizations will be documented in an EA report or other appropriate document concerning the activity involved. Monitoring A majority of the radio tracking and habitat survey data collected to date has been baseline information including the identification of seasonal ranges, reproduction areas, breeding areas and migration corridors. Future studies will place increasing emphasis on the monitoring of effects of increased human activity levels, particularly those associated with oil and gas exploration, on the wildlife species being studied. The management guidelines presented in this document are only partially based on monitoring information collected during the current studies on the Rocky Mountain Front. An important consideration in further monitoring efforts will be to test and validate the guidelines as to their effectiveness and applicability. PART A. General Management Guidelines The following general management guidelines are applicable coordination measures that will be considered when evaluating the effects of existing and proposed human activities in identified seasonally important habitats for a variety of wildlife species. 1. Identify and evaluate for each project proposal the cumulative effects of all activities, both existing uses and other planned projects. Potential site specific effects of the project being analyzed are a part of the cumulative effects evaluation which will apply to all lands within a designated biological unit. A biological unit is an area of land which is ecologically similar and includes all of the year long habitat requirements for a sub-population of one or more selected wildlife species. 2. Avoid human activities or combinations of activities on seasonally important wildlife habitats which may adversely impact the species or reduce the habitat effectiveness. -189- 3. Space concurrently active seismographic lines at least nine (9) air miles apart to allow an undisturbed corridor into which wildlife can move when displaced. One line survey crew will be allowed to work between active lines in order to reduce the total time of activity in any one area (Olson. G. 1981). 4. Establish helicopter flight patterns of not more than one-half (Jg) mile in width along all seismographic lines, between landing zones and the lines, and between landing zones and other operations, unless flying conditions dictate deviations due to safety factors. 5. Because helicopters produce a more pronounced behavioral reaction by big game and raptors than do fixed-wind aircraft, helicopters will maintain a minimum altitude of 600 feet (183 meters) above ground level when flying between landing zones and work areas where landing zones are not located on seismic lines, unless species specific guidelines recommend otherwise (Hinman, H., 1974; McCourt, K.H., et al 1974; Klein, D.R., 1973; Miller, F.L. and A. Guinn, 1979). 6. Designate landing zones for helicopters in areas where helicopter traffic and associated human disturbances will have the minimum impact on wildlife populations. Adequate visual and/or topographic barriers should be located between landing zones and occupied seasonal use areas. 7. The use of helicopters instead of new road construction to accomplish energy exploration and development is encouraged. 8. Base road construction proposals on a completed transportation plan which considers important wildlife habitat components and seasonal use areas in relation to road location, construction period, road standards, seasons of heavy vehicle use, road management requirements, etc. 9. Use minimum road and site construction specifications based on projected transportation needs. Schedule construction times to avoid seasonal use periods for wildlife as designated in the species specific guidelines. 10. Locate roads, drill sites, landing zones, etc. to avoid important wildlife habitat components based on a site specific evaluation. 11. Insert "dog-legs" or visual barriers on pipelines and roads built through dense vegetative cover areas to prevent straight corridors exceeding one-forth (h) mile where vegetation has been removed (Stubbs, C.W. and B.J. Markham, 1979). 12. Roads which are not compatible with area management objectives and are no longer needed for the purpose for which they were built will be closed and reclaimed. Native plant species will be used whenever possible to provide proper watershed protection on disturbed areas. Wildlife forage and/or cover species will be utilized in rehabilitation projects where deemed appropriate. 13. Keep roads which are in use during oil and gas exploration and development activity closed to unauthorized use. Place locked gates and/or road guards at strategic locations to deter unauthorized use when activities are occurring on key seasonal ranges. -190- 14. Impose seasonal closures and/or vehicle restrictions based on wildlife or other resource needs on roads which remain open. 15. Bus crews to and from drill sites to reduce activity levels on roads. Shift changes should be scheduled to avoid morning and evening wildlife feeding periods. 16. Keep noise levels at a minimum by muffling such things as engines, generators and energy production facilities. 17. Prohibit dogs during work periods. 18. Prohibit firearms during work periods or in vehicles traveling to and from work locations. 19. Seismographic and exploration companies should keep a daily log of activities. Items such as shift changes, shut dovm/start up times, major changes in noises or activity levels, and the location on the line where seismic crews are working should be recorded. PART B: Species Specific Management Guidelines The species specific management guidelines which follow provide coordination measures necessary to protect Important habitats or seasonal use areas for several wildlife species which were selected for intensive baseline surveys on the Rocky Mountain Front Study Area. Monitoring of the effects of human activities on these species and their habitats will continue to receive special study emphasis. Maps which delineate the seasonally Important habitats for which timing restrictions are specified have not been included in the management guideline document and are not available for general distribution. Copies of these maps are available for inspection at the offices of the four Agencies involved in the Rocky Mountain Front Wildlife Monitoring Program. These guidelines together with the "general management guidelines" will minimize, but not eliminate, the impacts of disturbances caused by human activities on these species. Species specific guidelines are currently available for grizzly bear, mountain goat, bighorn sheep, elk, mule deer and raptors. Grizzly Bear The Interagency Grizzly Bear Committee approved the application of guidelines on National Forest System, Bureau of Land Management (BLM) and National Park System lands throughout grizzly bear ecosystems in the States of Idaho, Montana, Washington, and Wyoming. (November 26, 1986 Federal Register, Vol. 51, No. 228). These guidelines are known as the Interagency Grizzly Bear Guidelines (IGBG). The IGBG provide definition and management direction for grizzly bear Management Situations I, II, III, iv and V and further provide generalized guidelines on how to coordinate various activities with the bear in the various management situations. Further, the IGBG were more specifically developed for the Yellowstone Ecosystem. -191- The Rocky Mountain Front Guidelines (RMFG) found in this document do not identify management situations or provide definitions or management directions of the stratification. The Management Situations designated on the Front pursuant to the IGBG identify where the emphasis on grizzly bear needs to be placed, and if there is a conflict, where the conflict should be resolved in favor of the bear; but the RMFG are the best management practices for coordinating multiple use activities with the grizzly bear on the Front. The RMFG are detailed coordination measures for specific activities that will assist land managers in meeting the management direction provided in the IGBG. Study results documented to date along the east Rocky Mountain Front are the basis for the development of management guidelines for grizzly bear and their habitat. During the period from 1977-1979, research was carried out by the Border Grizzly Project under a contract with the BLM. Since 1980 the Montana Department of Fish, Wildlife and Parks has assumed the intensive grizzly bear monitoring work with funding continuing from the Interagency Rocky Mountain Front Task Force private industry (American Petrofina, Williams Exploration, Sun Exploration) and the Nature Conservancy. In addition, a BLM funded livestock/grizzly bear interaction study was conducted by a graduate student from Montana State University during the field seasons of 1985 and 1986. These guidelines were developed as a direct result of grizzly bear monitoring conducted on the East Front. They represent guidelines that, when followed, will mitigate but not eliminate influences of human activities on grizzly bears and grizzly bear habitat. Human activities within grizzly bear range will have effects, however subtle, on grizzly bears. All previously mentioned "general management guidelines" are applicable coordination measures that should be considered when evaluating human activities in grizzly bear habitat. The following are additional species specific guidelines. 1. Avoid human activities in identified grizzly bear habitat constituent elements or portions of constituent elements containing specific habitat values during the following seasonal use periods (see data summarization): A. Spring habitat (concentrated use areas) April 1 - June 30 B. Alpine feeding sites July 1 - September 15 C. Subalpine f ir/whitebark pine habitat types— August 1 - November 30 D. Denning habitat October 15 - April 15. 2. Avoid human activities in grizzly bear habitat components which provide important food sources during spring and early summer, April 1 - July 15. These habitat components include riparian shrub types, Populus stands, wet meadows, sidehill parks, and avalanche chutes. Maintain an undisturbed zone of at least h mile between activities and the edge of these habitat components where many important bear foods occur. 3. Establish flight patterns in advance when activities require the use of helicopters. Flight patterns should be located to avoid seasonally important gjrizzly bear habitat constituent elements and habitat components during the designated seasonal use periods. -192- 4. 5. 6. 8. 9. 11. 12. No seismic or exploratory drilling activiti minimum of one mile of den sites during (Reynolds, P.E., et al, 1983). Seismic permits should include a clausfe temporary cessation of activities, if conflicts. es should be conducted within a the October 15 - April 15 period providing for cancellation or , to prevent grizzly /human necessary Scheduling of well drilling on adjacent bear use areas, should be staggered to displaced bears. sites, within important grizzly pijovide a disturbance free area for Pipeline construction required for the should be condensed into the shortest seasonal restrictions when conducted in development of a gas or oil field tjfme frame possible and subject to important grizzly bear habitat. Field operation associated with seismic should be placed carefully to avoid seasoii or constituent elements. Such placement avoid direct or potential conflicts between Retain frequent dense cover areas adjacebt and security cover necessary to protect Three sight distances are desirable grizzlies. A sight distance is the other large animal is essentially hidden vegetation cover. The same security timber harvest units. tto average or oil/gas exploration activities lally important habitat components of sites is necessary in order to man and grizzly bear. C(pver 10. No off-duty work camps will be allowed constituent elements. wil|hin occupied seasonally important Incinerate garbage daily or store in beat- local landfill dumps daily. Commercial activities permitted on publjic coordinated to avoid conflicts with grizz conducted under the monitoring program, trapping operations are active will be administrative actions by the agencies involved land should be planned and Ly bear trapping operations being general public use of areas where controlled through appropriate The following are grizzly bear management toward livestock grazing: Livestock grazing on Important spring deferred until after July 1. In pastures grazed after July 1, cattle shbuld of the riparian forage base is reduced by structural damage. -193- to roads for travel corridors Important habitat components, provide visual security for distance at which a grizzly or from the view of an observer by guidelines also applies to proof containers and remove to guidelines specifically oriented habitat for grizzly bears should be be removed before the amount 50 percent by either grazing or 3. Exceptions to the July 1 entry date can be made when a pasture is part of a grazing system (for example, rest rotation or deferred rest rotation) that does not cause a decrease in the condition or size of the riparian plant communities. 4. In riparian habitats that receive high amounts of bear use, fencing to exclude livestock grazing and trampling may be necessary. 5. Boneyards and livestock dumps are prevalent along the East Front and are frequented by grizzly bears. Ranchers and landowners should be encouraged to place carcasses of dead livestock and garbage on remote areas of their land. Dead cows and calves should be hauled a considerable distance from calving grounds to discourage bears from feeding on carion and newborn calves . 6. Options given in the IGBG for sheep allotments where grizzly - livestock depredation has been authenticated will be followed and include: (a) change the season of use, bedding practices, or grazing area to avoid known problem areas or other habitat important to grizzlies in time and space; (b) change the class of livestock from sheep to cattle if the range is suitable for cattle; or (c) remove all livestock and close the allotment. Vacant sheep allotments will not be restocked with sheep. In addition to the guidelines listed above for livestock grazing practices, the following research/management recommendations are presented: 1. The condition and trend of all riparian plant communities and their production of Angelica arguta, Heracleum lanatum, and Osmorhiza occidentalis need to be determined on all East Front public lands grazed by livestock. 2. For pastures where the condition of riparian plant communities needs improving, the construction of special use pastures is recommended. A special use pasture should be constructed where large areas of riparian vegetation are enclosed so an adequate forage base will be available to allow for stocking rates compatible with livestock operations. (Exclosures should be considered if riparian areas are too small.) These pastures should only be grazed after July 1, and the livestock should be removed before the special use pastures should be incorporated into a deferred rest rotation grazing system similar to that described by Marlow (1985). Some other methods which may be used to reduce impacts to riparian include; development of alternate water sources, placement of salt away from riparian, and improved herding practices. -194- For riparian areas where the abundance of grizzlies for cover (Populus tremuloides, or Betula spp.,) or food (Angelica arguta occidentalis) has been reduced, reestablis important plant species used by Populus tricocarpa, Salix spp., I Heracleum lanatum, or Osmorhiza ifiment should be attempted. Marlow, C.B. 1985. Controlling riparian zone Montana Agricultural Experiment Station. AgResearch 2(3): 1-7, 8072/2 damage with little forage loss. Moiitana State University. Montana ■ I -195-