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Table 2 Review of empirical evidence that disassortative mating contributes to the maintenance of genetic variation in kin recognition cues

From: Crozier’s paradox revisited: maintenance of genetic recognition systems by disassortative mating

Taxon

Cue used to facilitate assortative cooperation

Inbreeding avoidance/disassortative mating?

Cue used in mating choice

Potential for resolution of Crozier’s paradox by disassortative mating

References

Slime mould Dictyostelium discoideum

TgrB1 and TgrC1 surface proteins

Yes

mat locus

No

Benabentos et al. 2009 [13], Bloomfield et al. 2010 [49], Hirose et al. 2011 [46]

Fungi Neurospora crassa, Aspergillus heterothallicus, Sordaria brevicolus

MAT loci

Yes

MAT loci (lipopeptide pheromones)

Yes

Shiu and Glass 1999 [51], Aanen et al. 2008 [9], Hall et al. 2010 [52]

Fungi, other species

Other heterokaryon incompatibility loci

Yes

MAT loci (lipopeptide pheromones)

Possibly

Shiu and Glass 1999 [51], Aanen et al. 2008 [9], Hall et al. 2010 [52]

Colonial ascidians Botryllus schlosseri and Hydractinia symbiolongicarpus

Histocompatibility locus A

No

n/a

No

Grosberg and Quinn 1986, Grosberg and Hart 2000 [39], Rosengarten and Nicotra 2011 [14]

German cockroach Blattella germanica

CHCs

Yes

CHCs

Yes

Lihoreau et al. 2007 [59]; 2008 [60]; Lihoreau and Rivault 2008 [61]; 2010 [62]

Halictid bee Lasioglossum zephyrum

Lactones and/or CHCs

Yes

Lactones and/or CHCs

Possibly

Greenberg 1979 [72], Smith 1983 [68], Smith and Wenzel 1988 [73]

Social wasps Polistes dominulus and P. fuscatus

CHCs

Yes

Unknown

Possibly

Ryan and Gamboa 1986 [76], Gamboa 2004 [74], Liebert et al. 2010 [77]

Social wasp Ropalidia marginata

CHCs

No

n/a

No

Shilpa et al. 2010 [78]

Bumble bees Bombus spp.

Probably CHCs

In some species

Unknown

Possibly

Foster 1992 [69], Whitehorn et al. 2009 [79], Martin et al. 2010 [75]

Ants Leptothorax gredleri and Linepithema humile

CHCs

Yes

Probably CHCs

Possibly

Keller and Passera 1993 [70], Oppelt et al. 2008 [71], van Zweden and d’Ettorre 2010 [12]

Tuatara Sphenodon punctatus

MHC

Yes

MHC

Weak

Miller et al. 2009 [99]

Zebrafish Danio rerio

Odour cues

Yes

MHC-derived odours

Possibly

Gerlach and Lysiak 2006 [88], Gerlach et al. 2008 [89]

Arctic charr Salvelinus alpinus

MHC-derived odours

Yes

MHC-derived odours

Yes

Olsén et al. 1998 [95], Skarstein et al. 2005 [98]

Atlantic salmon Salmo salar

MHC-derived odours

Yes

MHC-derived odours

Yes

Landry et al. 2001 [90], Rajakaruna et al. 2006 [96]

Long-tailed tit Aegithalos caudatus

Contact calls

Yes

Unknown

Possibly

Hatchwell et al. 2000 [111], Sharp et al. 2005 [109]

Mouse Mus musculus

MHC-derived odours

Yes

MHC-derived odours

Yes

Yamazaki et al. 1976 [84], 1988 [85], 2000 [83], Potts et al. 1991 [87], Manning et al. 1992 [82]

Naked mole rat Heterocephalus glaber

Odour cues

Yes

Odour cues

Possibly

Clarke and Faulkes 1999 [114]

Mandrill Mandrillus sphinx

Odour cues

Yes

MHC-derived odours

Possibly

Charpentier et al. 2007 [11], Setchell et al. 2010 [116], 2011 [117]

Human Homo sapiens

Facial cues

Yes

Facial cues

Yes

DeBruine 2005 [122], Bailenson et al. 2008, DeBruine et al. 2008 [119], Krupp et al. 2008 [119], Nojo et al. 2011 [123]

  1. We list cases in which a cue used to facilitate assortative cooperation has been identified, state whether inbreeding avoidance or disassortative mating has been reported and examine whether the cues used in social and mate choice contexts are the same, potentially resolving Crozier’s paradox. CHCs: cuticular hydrocarbons, MHC: major histocompatibility complex.