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2015
DOI: 10.1002/ece3.1397
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Sexual segregation in North American elk: the role of density dependence

Abstract: We investigated how density-dependent processes and subsequent variation in nutritional condition of individuals influenced both timing and duration of sexual segregation and selection of resources. During 1999–2001, we experimentally created two population densities of North American elk (Cervus elaphus), a high-density population at 20 elk/km2, and a low-density population at 4 elk/km2 to test hypotheses relative to timing and duration of sexual segregation and variation in selection of resources. We used mu… Show more

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Cited by 16 publications
(13 citation statements)
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“…Hence, we propose that available habitat mediates the degree to which SSL sexual segregation is expressed, rather than individual-based limiting factors per se. Adult males breeding in Argentina were tracked from a substantially larger colony than the Falkland Islands (1300 pups versus 328 pups, respectively), so density dependence may also promote sexual segregation in Argentina through in creased intersexual competition, as is reported for terrestrial taxa (Campagna et al 2001, Stewart et al 2015.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Hence, we propose that available habitat mediates the degree to which SSL sexual segregation is expressed, rather than individual-based limiting factors per se. Adult males breeding in Argentina were tracked from a substantially larger colony than the Falkland Islands (1300 pups versus 328 pups, respectively), so density dependence may also promote sexual segregation in Argentina through in creased intersexual competition, as is reported for terrestrial taxa (Campagna et al 2001, Stewart et al 2015.…”
Section: Discussionmentioning
confidence: 99%
“…Sexual segregation in habitat use is ubiquitous in vertebrates and its influence on animal distribution, behaviour and survival can be profound (Ruckstuhl & N euhaus 2000, Jiménez et al 2015). Yet, while the ecological consequences of sexual segregation in habitat use are clear, the underlying causes are difficult to differentiate because critical tests of hypotheses are difficult to obtain (Ruckstuhl & N euhaus 2000, Main 2008, Stewart et al 2015.…”
Section: Introductionmentioning
confidence: 99%
“…We also estimated partial correlation coefficients between group-SSAS interpretations and TGS, controlling for population abundance; and between group-SSAS and population abundance, controlling for TGS [ 48 ]. Sexual segregation might be density-dependent [ 17 , 32 ]. Furthermore, typical group size is related to male abundance, and male abundance can be correlated to population abundance [ 49 ].…”
Section: Methodsmentioning
confidence: 99%
“…Associated with the wider forage niche of males is that males tend to show less site tenacity than females [ 30 ]. Furthermore, females, burdened with parental care, tend to select habitat that possesses fewer lethal risks [ 31 , 32 ]. Males, on the other hand, with a large body size, greater forage demands, and no burdens from parental care might use forage habitat with greater lethal risks [ 33 ].…”
Section: Introductionmentioning
confidence: 99%
“…Consequently, growth rate of horns or antlers is likely to be slower at higher densities than at lower densities with respect to nutritional carrying capacity because poor maternal nutrition can result in a negative maternal effect combined with limited resources available for growth of young and adult males. Among sexually dimorphic species, females compete largely with each other and young, and males compete with other males because the sexes segregate throughout much of the year (Bleich et al , Kie and Bowyer , Bowyer , Stewart et al ). For mountain sheep, young males typically remain with female groups until 2–4 years old when they disperse to join groups of males (Geist , Festa‐Bianchet , Bleich et al ).…”
Section: The Trifecta: Age Genetics and Nutritionmentioning
confidence: 99%