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92<br />

5.4. Results<br />

Habitat selection<br />

At the microhabitat scale, selecti on fo r <strong>de</strong>ns was obvious because juveniles were using<br />

<strong>de</strong>ns in 47% of observati ons while we never fo und <strong>de</strong>ns in the random locati ons we sampled<br />

(Fig. 5.1 a) . Juveniles also selected sites characteri zed by a hi gh protecti ve cover, low air<br />

temperature, and low wind speed (Fig. 5. l a, Table 5.1). The hazard rati os allowed us to<br />

quantify this selecti on and indicate that a 10% increase in protecti ve cover was associated<br />

with a 69% increase in selection, that a 1°C increase in temperature was associated with a<br />

2 1 % <strong>de</strong>crease in selecti on and that a 0.1 mis increase in wind speed was associated with a<br />

20% <strong>de</strong>crease in selection (Table 5.1). Wh en using a tree, juveniles selected <strong>la</strong>rge trees but<br />

did not signi ficantly use any tree species compared to aspens (Fig. 5. J b, Table 5. J).<br />

According to the hazard rati o, a 10 cm increase in the circumfe rence of the tree was<br />

associated with a 72% increase in selecti on (Table 5.1).<br />

At the local scale, juveniles selected areas with low herb cover and wi th cedar trees as<br />

dominant tree species (Fig. 5.2, Table 5.1). The hazard ratios indicate that a 10% increase in<br />

herb cover was associated with a 14% <strong>de</strong>crease in selecti on and that the presence of cedar as<br />

dominant tree species was associated with a J 36% increase in selection compared to when<br />

aspen was dominant (Table 5.1).

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