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61<br />

pattern of <strong>de</strong>n use over one or two winter seasons (n = 14 indivi<strong>du</strong>a1s followed from 23<br />

January to 14 April 2004; n = 6 indivi<strong>du</strong>als followed from 05 January to 19 March 2005;<br />

among which three indivi<strong>du</strong>als were followed both years). For that, we attached temperature<br />

loggers (SmartButton Temperature Loggers, ACR systems Inc.) to their radio col<strong>la</strong>r (total<br />

weight of col<strong>la</strong>r with temperature recor<strong>de</strong>rs = 74 g). We used abrupt changes in temperature<br />

readings to estimate the timing of movements in and out of the <strong>de</strong>ns. To complement data<br />

from temperature loggers, we p<strong>la</strong>ced movement d<strong>et</strong>ectors (Vigil 650X, Circuitronique Estrie<br />

Inc.) at the entrances of ail <strong>de</strong>ns used. Combining information from temperature loggers and<br />

movement d<strong>et</strong>ectors allowed us to d<strong>et</strong>ermine wh en animais were insi<strong>de</strong> or outsi<strong>de</strong> of a <strong>de</strong>n<br />

and therefore to ca\cu<strong>la</strong>te the time spent outsi<strong>de</strong> of the <strong>de</strong>n, the number and <strong>du</strong>ration of<br />

activity bouts, and the nocturnality in<strong>de</strong>x. The nocturnality in<strong>de</strong>x ln (after Zalewski 2000)<br />

reflects the re<strong>la</strong>tive distribution of activity b<strong>et</strong>ween day and night, and is calcu<strong>la</strong>ted as:<br />

2Nal<br />

1 = I N<br />

Il (Nal +(Dal<br />

I N) I D)<br />

(2)<br />

where Na and Da are total <strong>du</strong>ration of porcupine activity <strong>du</strong>ring night and day, respectively,<br />

and N and D are night and day lengths. Night started 30 min after sun s<strong>et</strong> and en<strong>de</strong>d 30 min<br />

before sunrise. In varies from 0 (diurnal activity) to 2 (nocturnal activity).<br />

Microhabitats used outsi<strong>de</strong> of the <strong>de</strong>n<br />

We mea<strong>sur</strong>ed habitat use by porcupines from 12 January to 16 April 2004 and Il January<br />

to 12 March 2005. Twice a week, we precisely located the 26 radiocol<strong>la</strong>red porcupines. For<br />

that, we followed the telem<strong>et</strong>ry signal to the animal (homing) instead of using triangu<strong>la</strong>tion.<br />

Each time we located an indivi<strong>du</strong>al, we assigned its position to one of the six microhabitats<br />

(i.e. "<strong>de</strong>n", "ground open", "ground covered" , "conifer open", "conifer covered" , or<br />

"<strong>de</strong>ci<strong>du</strong>ous"). If the animal was in a tree, we recor<strong>de</strong>d its position according to one of tluee<br />

c<strong>la</strong>sses of height (Iower third, middle, higher third of the canopy) and to one of two c<strong>la</strong>sses of<br />

distance to the trunk (base, tip of the branch). We also noted wh<strong>et</strong>her the porcupine was<br />

feeding or resting. We characterized thermal conditions in the stand by mea<strong>sur</strong>ing Tc using a<br />

hand held thermocouple (HH Il with type K thermocouple input, Omega Engineering Inc.,<br />

Stamford, Connecticut) inserted in a b<strong>la</strong>ck bowl and p<strong>la</strong>ced 0.3 m ab ove ground.

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