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American Bison - Buffalo Field Campaign

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composition and function, as well as being integrated into<br />

the larger landscape, and supporting sustainable human<br />

livelihoods. Ecological restoration involving bison as an integral<br />

component of ecosystems faces two major challenges: 1)<br />

how to undertake restoration across large areas with diverse<br />

land-use and ownership patterns; and 2) how to undertake<br />

restoration in a way that improves both biodiversity and human<br />

wellbeing. Large-scale ecological restoration involves biological<br />

and social complexity. Attitudes, economics and politics, from<br />

local to regional and international scales, will shape the future<br />

of bison conservation on occupied lands. These challenges are<br />

addressed in Chapter 10.<br />

1.5 Conserving the Wild Character and<br />

Genome of <strong>Bison</strong><br />

<strong>Bison</strong> in captive herds may be managed to achieve various<br />

objectives, including the ecological services that bison provide<br />

(e.g., grazing, nutrient cycling, and terrain disturbance),<br />

education and display, commercial production, and<br />

conservation of bison as wildlife. Conserving bison as wildlife<br />

is not necessarily served by managing a population for other<br />

purposes. For example, the ecological effects of herbivory may<br />

be achieved by grazing a variety of livestock species. Although<br />

some rangelands formerly used for cattle production have<br />

been converted to bison production, the substitution of bison<br />

for cattle production does not, by itself, necessarily contribute<br />

to bison conservation, or to ecological restoration of bison<br />

as wildlife. Similarly, display herds may serve conservation<br />

education objectives without otherwise contributing to species<br />

conservation.<br />

In the absence of intentional policies and actions to conserve<br />

the wild character and genome of bison, captivity and<br />

commercialisation can lead inadvertently or intentionally to<br />

a variety of effects that may be deleterious to bison as a<br />

wildlife species in the intermediate to long term (Chapter 4).<br />

These include effects on the genome: founder effect; reduced<br />

genetic diversity; persistence and phenotypic penetration<br />

of deleterious genes; or inadvertent selection for heritable<br />

morphology, tameness or adaptation to captivity. Small<br />

populations are particularly susceptible to such effects. The sex<br />

and age structure of captive conservation populations may be<br />

manipulated to reduce the risk of escape, remove aggressive<br />

animals, or to alter fecundity or the rate of population increase.<br />

The age composition of males in captive herds is typically<br />

substantially different from wild populations.<br />

The common practice in captive commercial herds of eliminating<br />

males, before they become morphologically and behaviourally<br />

mature, poses a challenging question about the roles of<br />

mate competition and natural selection for fitness in such<br />

populations. In general, selection pressures on captive wildlife<br />

are substantially different from those in the wild. O’Regan<br />

and Kitchener (2005) posited that domestication may occur<br />

inadvertently in captive wild mammals through passive selection<br />

for individuals behaviourally suited to captivity, with concomitant<br />

morphological changes over several generations. Most changes<br />

are thought to result from increasing paedomorphosis, whereby<br />

juvenile characteristics are retained in the adult form of an<br />

organism (O’Regan and Kitchner 2005). Clutton-Brock (1999)<br />

described changes in large mammals under captive conditions<br />

including reduced body and brain size, altered external<br />

appearance, the gaining of a fat layer beneath the skin and a<br />

reduction of the facial region. Inadvertent selection for tameness<br />

and adaptation to a captive environment is typical in mammals<br />

(Frankham et al. 1986), and in addition to altering “wildness”,<br />

can reduce the chances for successful reintroduction of captives<br />

into the wild. A loss of response to predators and alteration<br />

of defensive and sexual behaviours have also been reported<br />

in captive wildlife (Price 1999; 2002). Many commercial bison<br />

producers directly select for marketable traits such as early<br />

maturity, coat colour, body size and conformation. The latter<br />

“show ring traits” are promoted in bison industry advertisements,<br />

publications and at auctions.<br />

The large size of the commercial captive population is the basis<br />

for a popular misconception that the species is “secure”, leading<br />

wildlife management agencies to ignore actions necessary for<br />

conservation of wild type bison. Today, among North <strong>American</strong><br />

jurisdictions, there is a confusing array of classifications of bison<br />

as wildlife, domestic livestock, or both (Chapter 8).<br />

Hybridisation with cattle is another serious challenge for bison<br />

conservation. In the U.S., Canada, and Europe, agricultural<br />

interests attempted to develop an improved range animal by<br />

hybridising bison and cattle. Forced-mating of bison and cattle<br />

can be readily achieved in a controlled environment. However,<br />

they preferentially mate with their own species under open<br />

range conditions (Boyd 1908; Goodnight 1914; Jones 1907).<br />

In Europe, the European bison (<strong>Bison</strong> bonasus), a relative of<br />

the <strong>American</strong> bison, and the aurochs (Bos taurus primigeneus),<br />

progenitor of modern cattle, were sympatric, yet evolutionarily<br />

divergent, units. Typical of sympatric species occupying similar<br />

trophic niches, behavioural and ecological specialisation<br />

provides niche separation, leading to reproductive isolation<br />

and progressively to speciation (Bush 1975; Rice and Hostert<br />

1993). Species divergence and reproductive incompatibility<br />

are evident from the low fertility of first generation (F1) bison x<br />

cattle offspring (Boyd 1908; Steklenev and Yasinetskaya 1982)<br />

and the difficulty producing viable male offspring (Boyd 1914;<br />

Goodnight 1914; Steklenev and Yasinetskaya 1982; Steklenev et<br />

al. 1986). Unfortunately, forced hybridisations between B. bison<br />

and Bos taurus in North America have left a legacy of cattle<br />

mitochondrial (Polziehn et al. 1995; Ward et al. 1999) and nuclear<br />

DNA (Halbert 2003; Halbert et al. 2005). This introgression is<br />

<strong>American</strong> <strong>Bison</strong>: Status Survey and Conservation Guidelines 2010 3

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