2015
DOI: 10.13102/sociobiology.v62i1.116-119
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Clonal composition of colonies of a eusocial aphid, Ceratovacuna japonica

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Cited by 9 publications
(6 citation statements)
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“…As a result, it may undergo selection repeatedly in response to predation pressure. Indeed, Hattori et al 23 have shown that a colony consists of multiple clones. Adaptive defensive traits of soldiers should differ between populations with low and high predation pressure.…”
Section: Discussionmentioning
confidence: 99%
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“…As a result, it may undergo selection repeatedly in response to predation pressure. Indeed, Hattori et al 23 have shown that a colony consists of multiple clones. Adaptive defensive traits of soldiers should differ between populations with low and high predation pressure.…”
Section: Discussionmentioning
confidence: 99%
“…host-alternating) aphid that shows cyclic parthenogenesis characterized by several asexual phases and a sexual phase 22 . This species produces winged morphs for moving between its secondary host plant, Sasa senanensis (Poaceae: Bambuseae), and its primary host plant, Styrax japonicus (Styracaceae) 7 , 23 . This host-alternating behaviour can lead to clone mixing.…”
Section: Methodsmentioning
confidence: 99%
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“…These have shown that clonal mixing does occur within the galls, that the level of mixing is very variable, and that the dispersing aphids can adjust their social and reproductive behaviour depending on whether they are in their own gall or that of another clone (Abbot et al 2001; Johnson et al 2002; Wang et al 2008; Abbot 2009; Miller et al 2015). By contrast, there has been only one study of the genetic structure of soldier aphids in open colonies (Hattori et al 2015). This was on a very small scale (about 10 m x 5 m) and showed that there was some clonal mixing in five open colonies of Ceratovacuna japonica using AFLP markers (Hattori et al 2015).…”
Section: Introductionmentioning
confidence: 99%
“…These aphid species basically have a host-alternating life cycle; most of them induce galls on their primary host and form exposed colonies on their secondary host. Defensive individuals (usually first-or second-instar nymphs [2] but at times fourth-instar nymphs [8] or apterous adults [9,10]) have been recorded from the gall or the primary-host generations of all six tribes [9][10][11][12][13][14][15][16][17], and from the secondary-host generations of Eriosomatini [1], Cerataphidini [15,[18][19][20][21], and Hormaphidini [22]. Although exules of Paracletus cimiciformis (Fordini) have recently been shown to suck on ant larva hemolymph [23], defensive behavior on the secondary host has been unknown from the remaining three tribes to date.…”
Section: Introductionmentioning
confidence: 99%