Table 2. Evidence for introgression or shared ancestral polymorphism.
| Support for introgression | Support for ancestral polymorphism | Biological reason | 
|---|---|---|
| Species are know to hybridize under greenhouse conditions and in the wild | Species cannot hybridize under greenhouse conditions, and/or little evidence of hybridization in the wild | Strength of reproductive barrier dictates potential for hybridization and introgression | 
| Tightly linked genes show similar patterns of gene flow between species | Lack of correlation between allelic states at linked genes | Recombination less likely between linked genes, and introgressed linkage blocks are likely to be maintained | 
| Different patterns of genetic distances between species at different loci, with the greatest degree of divergence between loci contributing to species-level differences | Equal divergence across different loci | Selection pressures different for different loci, with strong diversifying selection at loci underlying species-specific traits | 
| Populations in sympatry or parapatry show less genetic divergence than those that occur in allopatry | Equivalent levels of divergence across species range | Where introgression occurs a cline of shared genes may be expected between species | 
| Phylogenetic incongruency between uniparentally and biparentally inherited markers | Congruency between the phylogeny derived from uniparentally inherited markers and the maximum clade credibility tree from biparentally inherited markers | Uniparentally inherited markers (thus with a low effective population size) are particularly susceptible to introgression | 
Data from Willyard et al. (2009); Yatabe et al. (2007) and Donnelly et al. (2004).