Proceedings of the Seventh Mountain Lion Workshop
Proceedings of the Seventh Mountain Lion Workshop
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>