group |
sexual selection measure studied |
speciation effect |
claim |
authority |
birds (passerines) |
sexual dichromatism |
increased species richness |
sexual selection drives speciation |
Barraclough et al. (1995, 1998) |
|
sexual dichromatism |
no effect |
|
Price (1998) (part of same data set as above) |
birds |
mating system |
increased species richness |
sexual selection drives speciation |
Mitra et al. (1996) |
birds |
ornamented versus non-ornamented |
increased species richness |
sexual selection drives speciation |
Møller & Cuervo (1998) |
birds |
sexual dichromatism |
increased species richness |
sexual selection drives speciation |
Owens et al. (1999) |
|
sexual dimorphism |
no effect |
|
|
|
mating system |
no effect |
|
|
birds |
sexual size dimorphism |
no effect |
increased speciation due to sexual conflict may be countered by increased extinction |
Morrow et al. (2003a) |
|
sexual dichromatism |
no effect |
|
|
|
testis size |
no effect |
|
|
insects: Coleoptera, Diptera, Ephemeroptera, Homoptera, Lepidoptera |
monandry versus polyandry |
increased species richness under polyandry |
postcopulatory sexual conflict drives speciation |
Arnqvist et al. (2000) |
insects: Syrphidae (Diptera) |
spermathecal width |
increased species richness |
postcopulatory sexual conflict drives speciation |
Katzourakis et al. (2001) |
|
testis length |
increased species richness |
|
|
insects: Papuan butterflies |
sexual size dimorphism |
no effect |
species richness may arise through allopatry |
Gage et al. (2002) |
|
mating frequency |
no effect |
|
|
spiders |
sexual size dimorphism |
no effect |
species richness may arise through allopatry |
Gage et al. (2002) |
mammals |
sexual size dimorphism |
no effect |
species richness may arise through allopatry |
Gage et al. (2002) |
|
testis size |
no effect |
|
|
fish: Goodeinae |
sexual size dimorphism |
no effect |
species richness may arise primarily through allopatry and ecological divergence |
Ritchie et al. (2005) |