2020
DOI: 10.1016/j.anbehav.2020.03.014
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Alliance-specific habitat selection by male Indo-Pacific bottlenose dolphins in Shark Bay, Western Australia

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Cited by 12 publications
(5 citation statements)
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“…We did not include male age in our analyses because age is a significant predictor of alliance formation, i.e., second-order allies tend to be of a similar age ( 27 ), age does not influence a male’s number of paternities ( 25 ), and mature males of all ages participate in third-order alliances ( 24 , 29 ). We have suggested that alliance partners are selected strategically based on social and ecological homophily, because alliances with broadly overlapping ranges differ in preferred foraging habitat and behavior (( 37 , 38 ), see SI Appendix ). Our finding that second-order alliance size is unrelated to consortship rate and duration is unsurprising if second-order alliance size is related to alliance variation in foraging behavior ( 38 ) and perhaps demographic variation in the availability of potential partners.…”
Section: Discussionmentioning
confidence: 99%
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“…We did not include male age in our analyses because age is a significant predictor of alliance formation, i.e., second-order allies tend to be of a similar age ( 27 ), age does not influence a male’s number of paternities ( 25 ), and mature males of all ages participate in third-order alliances ( 24 , 29 ). We have suggested that alliance partners are selected strategically based on social and ecological homophily, because alliances with broadly overlapping ranges differ in preferred foraging habitat and behavior (( 37 , 38 ), see SI Appendix ). Our finding that second-order alliance size is unrelated to consortship rate and duration is unsurprising if second-order alliance size is related to alliance variation in foraging behavior ( 38 ) and perhaps demographic variation in the availability of potential partners.…”
Section: Discussionmentioning
confidence: 99%
“…We have suggested that alliance partners are selected strategically based on social and ecological homophily, because alliances with broadly overlapping ranges differ in preferred foraging habitat and behavior (( 37 , 38 ), see SI Appendix ). Our finding that second-order alliance size is unrelated to consortship rate and duration is unsurprising if second-order alliance size is related to alliance variation in foraging behavior ( 38 ) and perhaps demographic variation in the availability of potential partners. However, we have shown that the strategic investment in third-order alliance relationships does increase access to a contested resource, through an increase in the duration of consortships.…”
Section: Discussionmentioning
confidence: 99%
“…The shallow and protected estuary habitat provides resources that allow dolphins to reside year-round, with prey availability being continuous and more dependable than that in coastal habitats (McCluskey et al 2016). Habitat and prey selection is therefore likely to influence how dolphins associate (Holyoake et al 2010;O'Brien et al 2020;McCluskey et al 2021;Nicholson et al 2021).…”
Section: Discussionmentioning
confidence: 99%
“…The male bottlenose dolphins in Shark Bay participate in up to three levels or orders of alliances in a large, open society of resident dolphins with a dynamic fission–fusion grouping pattern (Connor and Krützen 2015 ; Gerber et al 2020 , 2021 ; King et al 2021 ). Males have larger ranges than females but retain their natal range in their adult home range (Connor et al 2000 ; Krützen et al 2004 ; Tsai and Mann 2013 ) and both sexes exhibit a continuous mosaic of overlapping home ranges (Watson-Capps 2005 ; Randić et al 2012 ; O’Brien et al 2020 ). Second-order alliances contain 4–14 males, may endure for decades, and are considered the core unit of male social organization in Shark Bay.…”
Section: Introductionmentioning
confidence: 99%