Table 6.1 Diets of plains bison at select locations within North <strong>American</strong> ecoregions. Ecoregion Location Season Northern Mixed Grasslands Central Shortgrass Prairie Tall Grasslands Prairie and Southern Shortgrass Prairie Northern Fescue Grasslands Rocky Mountain Forests Northern Forests Wind Cave NP, SD Pawnee Site, CO Lightly grazed Heavily grazed Wichita Mountains NWR, OK Tallgrass Prairie Preserve, OK National <strong>Bison</strong> Range, MT Yellowstone Northern Range,WY Yellowstone Central Range, WY Elk Island NP, AB Prince Albert NP, SK Grasses (%) Sedges (%) 44 <strong>American</strong> <strong>Bison</strong>: Status Survey and Conservation Guidelines 2010 Plant Type Forbs (%) Woody Plants (%) Others (%) Reference Spring 81 7 9 3 Marlow et al. 1984 Summer 79 9 10 2 Autumn 77 12 6 5 Winter 79 12 2 7 Winter 59 37 4 Spring 98 2 Summer 94 5 Autumn 99 Winter 94 4 Spring 95 4 Summer 96 4 Autumn 87 2 12 Winter 81 6 11 Spring & Summer Westfall et al. 1993 Wydevan and Dahlgren 1985 Peden et al. 1974 Peden et al. 1974 99 Buechner 1950 Spring 60 39 1 Summer 88 11 1 Autumn 84 16 1 Winter 79 21 1 Coppedge et al. 1998 Annual 90 1 2 1 McCullough 1980 Winter 53 44 1 1 1 Summer 55 37
6.2.1.2.1 Northern mixed grasslands In the absence of fire, bison have been observed making extensive use of prairie dog colonies in the northern mixed grasslands ecoregion, where colonies may have covered 2- 15% of the short grasslands (Knowles et al. 2002; Virchow and Hygnstrom 2002). <strong>Bison</strong> utilise the forb-dominated centres of prairie dog colonies for resting and wallowing, but feed at the graminoid-dominated periphery of colonies rather than at the colony centre (Coppock and Detling 1986; Krueger 1986). <strong>Bison</strong> use of prairie dog towns peaks during the summer and declines in the autumn (Krueger 1986) when the available forage biomass is low or the vegetation is senescent (Coppock et al. 1983a; 1983b). <strong>Bison</strong> use of colony sites also declines when recently burned grasslands are available (Coppock and Detling 1986). Grasses and sedges were almost 90% of the year-round bison diet, and sedges formed 7 to 37% of the seasonal diet in the northern mixed grassland ecoregion (Table 6.1). <strong>Bison</strong> selected foraging sites containing more than 75% warm season (C4) grasses during the summer growing season (Steuter et al. 1995). C4 grasses were approximately 33% of the diet in June, and a maximum of 40% of the bison diet in late summer, but C4 grasses were less in the bison diet in autumn, winter, and spring (Plumb and Dodd 1993). Conversely, cool season grasses formed approximately 50% of the summer diet, but increased to 80% of the diet in September (Plumb and Dodd 1993). 6.2.1.2.2 Central shortgrass prairie In a lightly grazed site, bison almost exclusively consumed grasses, but consumed more than 10% woody plants in the autumn and winter at a heavily grazed central shortgrass prairie site shared with cattle and sheep (Table 6.1). Three C4 grasses accounted for 65 to 75% of the bison diet (Peden et al. 1974; Schwartz and Nagy 1976). 6.2.1.2.3 Tall grasslands prairie and southern shortgrass prairie <strong>Bison</strong> in the tall grasslands prairie and southern shortgrass prairie ecoregions utilised only recently burned areas in spring, but selected areas burned annually throughout the year (Shaw and Carter 1990; Vinton et al. 1993). <strong>Bison</strong> grazing and regrazing can maintain areas with a low vegetative cover and standing crop (Coppedge and Shaw 1998; Vinton et al. 1993). Areas grazed by bison were characterised by a lower abundance of C4 grasses, a higher abundance of C3 grasses, and greater overall plant species diversity (Hartnett et al. 1996). These characteristics were more pronounced in areas burned annually (Hartnett et al. 1996), which is consistent with greater bison use of annually burned sites (Shaw and Carter 1990; Vinton et al. 1993). <strong>Bison</strong> grazed little bluestem (Schizachyrium scoparium) more frequently post-burning, probably in response to removal of standing dead tillers by fire (Pfieffer and Hartnett 1995). The greater overall plant species diversity in burned areas was linked to increased nitrogen cycling and availability (Bakker et al. 2003; Johnson and Matchett 2001). C3 grasses were the most common dietary item in winter (Coppedge et al. 1998). Dietary quality, as measured by faecal nitrogen, peaked in May and June, coincident with a peak in C3 grasses productivity (Post et al. 2001). Up to 39% of the spring diet was sedges (Coppedge et al. 1998). 6.2.1.2.4 Northern fescue grasslands Understanding contemporary trophic ecology of bison in this ecoregion is confounded somewhat by a management-imposed rotational grazing, by which bison are moved throughout the National <strong>Bison</strong> Range (NBR) National Wildlife Refuge, Montana (McCullough 1980). When occupying lower elevation areas of the NBR, bison utilised level to undulating open grasslands. Once herded to higher elevation portions of the range, bison continued to utilise the more level open areas available (McCullough 1980). The year-round distribution of bison was away from higher elevation steep-slope areas. <strong>Bison</strong> showed no selection for aspect, as they tended to use the more level areas available throughout the year. <strong>Bison</strong> fed almost exclusively on grasses (Table 6.1; McCullough 1980). 6.2.1.2.5 Rocky Mountain forest In the high topographical relief of the Rocky Mountains the heterogeneity of herbaceous productivity and standing crop is caused by the spatial distribution of moisture on the landscape. Herbaceous above ground net primary productivity (ANPP) is influenced by site-specific topographic position relative to moisture distribution and aspect (Burroughs et al. 2001). Herbaceous ANPP is lower at low elevations with less precipitation and at the highest elevations due to a shorter growing season attributable to lower temperatures than at mid- elevations (Coughenour 2005). In general, herbaceous ANPP occurs as a pulse of nitrogen rich vegetation that sequentially follows an elevational gradient from the lower elevation winter ranges to the higher elevation summer ranges. This pattern of ANPP makes young nutritious and concentrated forage available to bison for up to six months of each year (Frank and McNaughton 1992). Summer movements of bison to higher elevation areas reduces vegetation utilisation at lower elevations and thereby enhances the availability of vegetation at lower elevations during the non-growing season (Frank and McNaughton 1992). <strong>Bison</strong> on Yellowstone’s northern range forage on sedges within more mesic sites in winter (Meagher 1973) to the extent that the winter diet is more than 95% grasses, sedges, and rushes (Table 6.1; Singer and Norland 1994). Similarly, bison utilising the Yellowstone central range during winter primarily feed on sedges along the edges of thermally influenced drainages and <strong>American</strong> <strong>Bison</strong>: Status Survey and Conservation Guidelines 2010 45
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American Bison Status Survey and Co
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American Bison Status Survey and Co
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Table of Contents Acknowledgements
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6.3 Demographics ..................
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9.6 Active Management: Handling, He
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northern bison herds, managers shou
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may not have been validated. Testin
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2) A tendency to flee if approached
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2. Determine the required scope of
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Chapter 10 Guidelines for Ecologica
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anywhere without engaging stakehold
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Interventions (e.g., supplemental f
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Agabriel, J. and Petit, M. 1996. Qu
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Byerly, R.M., Cooper, J.R., Meltzer
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Dragon D.C. and Rennie, R.P. 1995.
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Gilpin, M.E. and Soulé, M.E. 1986.
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Joern, A. 2005. Disturbance by fire
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Matthews, S.B. 1991. An assessment
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Possingham, H.P., Davies, I., Noble
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Shaw, J.H. 1995. How many bison ori
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van Zyll de Jong, C.G. 1986. A Syst
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Appendix A North American conservat
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Plains bison (continued) State/Prov
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INTERNATIONAL UNION FOR CONSERVATIO