Table 2

Many of the documented examples of speciation in natural species fit the proposed model.

Species

Nature of the phenotype associated to speciation

Population structure and mutation load


Fish


Salmonidae

Highly philopatric

Studies on MHC give conflicting results suggesting optimal outbreeding model


Cichlids

Bright colours typical of species are recessive (disappear in hybrids)

Close preference for kin, with no detectable inbreeding depression


Sticklebacks

EDA mutation (armour plate loss) is completely recessive

Pitx1 mutation (loss of pelvic structures) is recessive

Studies on MHC support optimal outbreeding model


Panmictic species (cod, macquerel, tuna...)

Susceptible to large and unpredictable fluctuations in numbers


Birds

Migrating birds are highly philopatric


Quail

Preferential mating among cousins (led to Bateson's optimal oubreeding)


Darwin's finches

High inbreeding coefficient due to small size of the niche


Mammals

Rate of speciation inversely related to the effective size of populations


Mice and rats

Very fragmented populations correlates with capacity to inbreed


Pikas

Optimal outbreeding


Insects


Haplodiploids (bees, ants, termites)

Very low mutations loads correlate with very high species richness, and global ecological success


Drosophila

Mating preferences are recessive (disappear in F1)

Assortative mating, and chromosomal rearrangements are more prominent between populations that are in close contact in the wild.

H. Carson highlighted the correlation of speciation with small populations based mostly on data from drosophila.


Apple maggot fly

Fruit preference is recessive (disappears in F1)


Heliconius mimetic butterflies

Sexual preference of the males is asymmetric, and linked to the recessive yellow colour


Plants

Selfing plants undergo more speciation, but the species go extinct more quickly


Monkey flowers

The red derived phenotype is recessive to the pink ancestral one


Please refer to text in section V for relevant bibliographic references

Joly Biology Direct 2011 6:62   doi:10.1186/1745-6150-6-62

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