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Proceedings of the Seventh Mountain Lion Workshop

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154 DISPERSAL IN MALE PUMAS · Laundré and Hernández<br />

mating with sisters or mo<strong>the</strong>rs that have<br />

shifted <strong>the</strong>ir home range areas. This<br />

minimal distance should be represented by<br />

<strong>the</strong> average dispersal distance <strong>of</strong> females<br />

(sisters) from <strong>the</strong>ir natal home range.<br />

RESULTS<br />

Prediction #1: Male conflicts<br />

Relative to levels <strong>of</strong> adult male/kitten<br />

conflict or infanticide, we found ample<br />

evidence for infanticide in our study and in<br />

<strong>the</strong> literature. We recorded 4 cases <strong>of</strong> adult<br />

male pumas killing kittens (9 kittens total) in<br />

our study area. Robinette et al. (1961) cited<br />

reports from Utah <strong>of</strong> young pumas being<br />

killed by adult males on 2 occasions.<br />

Hornocker (1970) reported 1 instance <strong>of</strong> an<br />

adult male killing 2 kittens in his study area<br />

in central Idaho. Lindzey et al. (1989)<br />

reported 4 kittens being killed by pumas in<br />

sou<strong>the</strong>rn Utah. However, <strong>the</strong>y were not sure<br />

<strong>of</strong> <strong>the</strong> sex <strong>of</strong> <strong>the</strong> responsible animals.<br />

Spreadbury et al. (1996) documented 2 male<br />

kittens being killed by a transient male in<br />

British Columbia. Logan and Sweanor<br />

(2001) reported 12 kittens being killed by<br />

adult males in <strong>the</strong>ir study in New Mexico.<br />

With respect to adult male/subadult male<br />

conflicts, Lindzey et al. (1989) reported a<br />

transient male being cannibalized by a<br />

resident male. Murphy (1998) reported 2<br />

incidences <strong>of</strong> territorial males killing<br />

yearling males in his study in Yellowstone<br />

National Park. Logan and Sweanor (2001)<br />

reported 4 mortalities <strong>of</strong> younger (14.3-21<br />

months) males being killed by older males,<br />

including 1 instance <strong>of</strong> a fa<strong>the</strong>r killing his<br />

son.<br />

Although Hornocker (1970) and<br />

Seidensticker et al. (1973) did not report<br />

conflicts among adult male pumas, various<br />

o<strong>the</strong>r investigators reported it as ra<strong>the</strong>r<br />

common. In our area, adult males we<br />

captured <strong>of</strong>ten had facial scars and torn ears,<br />

presumably from conflicts with o<strong>the</strong>r adult<br />

males or, perhaps, females. Sitton and<br />

PROCEEDINGS OF THE SEVENTH MOUNTAIN LION WORKSHOP<br />

Weaver (1977) reported 2 adult pumas being<br />

killed by o<strong>the</strong>r adult pumas as a result <strong>of</strong><br />

fighting. However, <strong>the</strong> sex <strong>of</strong> <strong>the</strong><br />

combatants was unknown. McBride (1976)<br />

reported 2 incidences <strong>of</strong> adult males with<br />

extensive facial injuries and 1 instance <strong>of</strong> an<br />

adult male being killed by ano<strong>the</strong>r. Murphy<br />

(1998) reported an adult immigrant male<br />

being killed by <strong>the</strong> resident male. Logan<br />

and Sweanor (2001) found 5 adult males<br />

killed by o<strong>the</strong>r males. They also reported<br />

that 4 <strong>of</strong> <strong>the</strong> 5 winners outweighed <strong>the</strong><br />

losers, 2 <strong>of</strong> <strong>the</strong> 5 losers were killed by older<br />

animals, and 2 <strong>of</strong> <strong>the</strong> o<strong>the</strong>r 3 were 8 and 12<br />

years old, well past <strong>the</strong>ir prime.<br />

Prediction # 2: occurrence <strong>of</strong> inbreeding<br />

Concerning <strong>the</strong> presence <strong>of</strong> inbreeding<br />

within puma populations, it is well known<br />

that <strong>the</strong> Florida pan<strong>the</strong>r is highly inbred,<br />

including first order matings (Roelke et al.<br />

1993, Barone et al. 1994 and o<strong>the</strong>rs). This<br />

indicates that <strong>the</strong>re is no innate “aversion” to<br />

inbreeding. Logan and Sweanor (2001)<br />

reported an average residency <strong>of</strong> males <strong>of</strong> 6<br />

years (maximum = 8 yrs) in <strong>the</strong>ir study in<br />

New Mexico. If we assume an average <strong>of</strong> 2<br />

years per litter (Logan and Sweanor 2001),<br />

males were resident on average for at least 3<br />

generations. Given that females are<br />

primarily philopatric (Logan and Sweanor<br />

2001), and <strong>the</strong>re is no aversion to inbreeding<br />

with <strong>the</strong>ir fa<strong>the</strong>rs, we predict that with this<br />

length <strong>of</strong> residency a fa<strong>the</strong>r would have <strong>the</strong><br />

opportunity to mate twice with his daughters<br />

and once with granddaughters. If <strong>the</strong>re is an<br />

innate aversion to inbreeding, such matings<br />

should not occur. Logan and Sweanor<br />

(2001) report that 2 females mated with <strong>the</strong>ir<br />

fa<strong>the</strong>rs, 1 <strong>of</strong> <strong>the</strong>m mated with her fa<strong>the</strong>r<br />

twice, supporting <strong>the</strong> prediction based on no<br />

aversion to inbreeding.<br />

Prediction # 3: Dispersal distances<br />

For dispersal distances <strong>of</strong> males, we<br />

limited our analysis to animals that were<br />

known to have set up territories or were

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