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Proceedings of the Seventh Mountain Lion Workshop

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Sweanor 2001) could easily dominate over<br />

<strong>the</strong>ir smaller mo<strong>the</strong>r or sisters. As males do<br />

not seem reluctant to mate with close<br />

relatives, i.e. daughters, why don’t <strong>the</strong>y wait<br />

around to mate with <strong>the</strong>ir sisters or mo<strong>the</strong>rs?<br />

We conclude that <strong>the</strong> only logical answer to<br />

this question is that <strong>the</strong> high level <strong>of</strong> conflict<br />

with <strong>the</strong>ir fa<strong>the</strong>rs or, by default, even more<br />

competitive older bigger new male arrivals<br />

(who have displaced <strong>the</strong>ir fa<strong>the</strong>rs), force<br />

young males to disperse out <strong>of</strong> <strong>the</strong>ir natal<br />

area at an age (13-15 months <strong>of</strong> age) before<br />

<strong>the</strong>y are sexually mature (Sweanor 1990).<br />

Regarding prediction #3, <strong>the</strong> observed<br />

frequency distribution <strong>of</strong> HRDs was best fit<br />

by <strong>the</strong> competition model with a p(0) = 0<br />

and an increasing p(x) until a distance <strong>of</strong> 5<br />

HRDs. This model would reflect <strong>the</strong> effect<br />

<strong>of</strong> an increasing competitive ability <strong>of</strong> <strong>the</strong><br />

young males as <strong>the</strong>y disperse. In contrast, it<br />

is obvious that <strong>the</strong> data do not fit <strong>the</strong> most<br />

critical part <strong>of</strong> <strong>the</strong> inbreeding avoidance<br />

model: males should not settle within 2<br />

HRDs <strong>of</strong> <strong>the</strong>ir natal home range.<br />

Additionally, considering that even 5 HRDs<br />

may not be sufficient to reduce <strong>the</strong> chance <strong>of</strong><br />

inbreeding with sisters (Shields 1987,<br />

Sweanor 1990), <strong>the</strong> high percent (>50%) <strong>of</strong><br />

settlements within <strong>the</strong> first 4 HRDs argues<br />

strongly against inbreeding avoidance being<br />

<strong>the</strong> driving force behind male dispersal.<br />

The decreasing number <strong>of</strong> settlements<br />

between 5 and 7 HRDs likely reflects <strong>the</strong><br />

fragmented nature <strong>of</strong> <strong>the</strong> 2 studies that<br />

contributed <strong>the</strong> majority <strong>of</strong> <strong>the</strong> data (54.2 %;<br />

Logan and Sweanor 2001 and this study). In<br />

both studies, <strong>the</strong> principal mountain range(s)<br />

<strong>of</strong> <strong>the</strong> study areas are separated from nearby<br />

larger mountain ranges (places young pumas<br />

are most likely to find vacant territories) by<br />

valleys 75 to 100 + km wide. Thus, <strong>the</strong>re is<br />

a reduced likelihood <strong>of</strong> a male puma finding<br />

a territory in <strong>the</strong> 5-7 HRD range.<br />

Although nei<strong>the</strong>r model predicted <strong>the</strong><br />

higher number <strong>of</strong> settlements we found at >9<br />

and up to 20 HRDs, this finding also does<br />

DISPERSAL IN MALE PUMAS · Laundré and Hernández 157<br />

PROCEEDINGS OF THE SEVENTH MOUNTAIN LION WORKSHOP<br />

not support <strong>the</strong> inbreeding avoidance<br />

hypo<strong>the</strong>sis. If a young male was dispersing<br />

primarily to avoid inbreeding, we would not<br />

predict such long distance dispersals where<br />

animals passed up what would appear to be<br />

ample suitable habitat in <strong>the</strong>ir dispersal<br />

movements. The only explanation for such<br />

long distance dispersals is <strong>the</strong>y had to<br />

continue to travel because <strong>the</strong>y were outcompeted<br />

by resident males or transients<br />

that had traveled fur<strong>the</strong>r than <strong>the</strong>mselves.<br />

Eventually, <strong>the</strong>y would gain weight and<br />

experience enough to successfully compete<br />

for a territory (Sweanor 1990).<br />

Sweanor (1990) originally suggested that<br />

male residency times, <strong>the</strong> polygynous<br />

mating system, and male dispersal distances<br />

in pumas argued against inbreeding<br />

avoidance being <strong>the</strong> main driving force in<br />

dispersal <strong>of</strong> young male pumas. However,<br />

after presenting fur<strong>the</strong>r evidence <strong>of</strong><br />

aggression among male pumas and<br />

inbreeding between fa<strong>the</strong>rs and daughters,<br />

Logan and Sweanor (2001) concluded that<br />

inbreeding avoidance was likely <strong>the</strong> main<br />

driving force behind male puma dispersal.<br />

Their argument centered on <strong>the</strong> assumption<br />

that young males should only disperse far<br />

enough to “avoid” competition. We contend<br />

that with 15 - 18 % <strong>of</strong> puma populations<br />

being primarily transient males (Hemker et<br />

al. 1984, Ross and Jalkotzy 1992,<br />

Spreadbury et al. 1996, Laundré and Clark<br />

2003), no dispersing male ever has <strong>the</strong><br />

luxury <strong>of</strong> avoiding competition for a<br />

territory. They concurred with <strong>the</strong> presence<br />

<strong>of</strong> <strong>the</strong>se transients and observed that new<br />

males were constantly coming into <strong>the</strong>ir<br />

population and concluded from this that<br />

competition must be “tolerable”. They<br />

fur<strong>the</strong>r argued that under <strong>the</strong> competition<br />

hypo<strong>the</strong>sis, however, most <strong>of</strong> <strong>the</strong> male<br />

recruits in <strong>the</strong>ir growing population should<br />

have been <strong>of</strong>fspring <strong>of</strong> <strong>the</strong> area. Because in<br />

<strong>the</strong>ir study most male recruits came from<br />

outside, <strong>the</strong>y argued that this refuted <strong>the</strong>

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