1986
DOI: 10.1038/322456a0
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The genetic control and consequences of kin recognition by the larvae of a colonial marine invertebrate

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Cited by 271 publications
(216 citation statements)
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References 31 publications
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“…Buss (1982) suggested that the increased size of chimeras over clones would benefit chimeras when sizespecific ecological processes, such as competitive ability, predation risk and fecundity, existed. In support of this, larger size increases growth rate and survival in B. schlosseri and in corals that are known to form chimeras with close kin (Hughes & Jackson 1980;Jokiel & Morrissey 1986;Grosberg & Quinn 1986). In addition, a recent study has shown that grouping by sperm in wood mice increases swimming velocity (Moore et al 2002).…”
Section: Discussionmentioning
confidence: 97%
“…Buss (1982) suggested that the increased size of chimeras over clones would benefit chimeras when sizespecific ecological processes, such as competitive ability, predation risk and fecundity, existed. In support of this, larger size increases growth rate and survival in B. schlosseri and in corals that are known to form chimeras with close kin (Hughes & Jackson 1980;Jokiel & Morrissey 1986;Grosberg & Quinn 1986). In addition, a recent study has shown that grouping by sperm in wood mice increases swimming velocity (Moore et al 2002).…”
Section: Discussionmentioning
confidence: 97%
“…Indeed, self-matching may be favoured in nepotistic situations, in which animals need to identify individuals to whom they are most closely related (e.g. Getz & Smith 1986;Grosberg & Quinn 1986;Manning et al 1992;Petrie et al 1999). In contrast, additional referents (such as parents and siblings) should be used in mate-choice decisions, to help animals identify all individuals to whom they are closely related (e.g.…”
Section: Introductionmentioning
confidence: 99%
“…To the extent that this specificity is genetically controlled, the loci governing invertebrate allorecognition specificity may exhibit polymorphism that rivals, or exceeds, levels recorded at loci in the vertebrate Major Histocompatibility Complex (Potts and Wakeland 1990;Hughes and Nei 1992;Brown and Ecklund 1994;Hedrick 1994), as well as loci associated with gametophytic incompatibility systems in angiosperms (Ebert et al 1989). High levels of allotypic specificity could, however, result from any number of genetic alternatives, ranging from one or a few loci with tens to hundreds of alleles per locus (characteristic of populations of botryllid ascidians : Milkman 1967;Mukai and Watanabe 1975a,b;Scofield et al 1982;Grosberg and Quinn 1986;Rinkevich and Saito 1992;Yund and Feldgarden 1992;Rinkevich et al 1994) to numerous independent loci with relatively low levels of allelic variation (Curtis et al 1982). The ability to distinguish among these genetic alternatives, and to circumscribe the rules governing compatibility, determines how the expression of allorecognition-dependent behaviors influences the evolution of allotypic variation.…”
Section: Simulated Frequencies Of Compatibility In Full and Halfmentioning
confidence: 99%
“…No studies comprehensively quantify these costs and benefits. Moreover, because the genetic polymorphism that characterizes most invertebrate allorecognition systems should restrict fusion to close relatives and aggression to more distantly related individuals, the costs and benefits of both types of behavior must be adjusted according to kinship of the interactants (Buss and Green 1985;Grosberg and Quinn 1986;Reeve 1989;Grafen 1990), an unknown quantity in most instances.…”
Section: 0 -R ---------------mentioning
confidence: 99%