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 | |
Arctic charr Salvelinus alpinus | MHC-derived odours | Yes | MHC-derived odours | Yes | |
Atlantic salmon Salmo salar | MHC-derived odours | Yes | MHC-derived odours | Yes | |
Long-tailed tit Aegithalos caudatus | Contact calls | Yes | Unknown | Possibly | |
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] |