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The frequency of outcrossing in two hybridizing species of Iris was estimated for populations and for individual fruits. Effects of floral phenology and the local densities of flowers on outcrossing rates were examined and the potential for hybrid seed formation under different pollen environments was assessed. The populations examined differed with respect to the spatial distribution of plants and the level of genetic structure; the I. fulva population consisted of a number of low density patches and appeared to have some genetic differentiation whereas the I. hexagona population consisted of a single high-density experimental plot of randomly distributed genotypes. Population outcrossing rate estimates were relatively high (0.67-0.90) for both species. The distribution of family outcrossing rates tended to be bimodal for both species with individual fruits either having the majority of seeds fertilized by outcrossed donors or being almost entirely selfed. fulva may have been a consequence of higher levels of vegetative reproduction and genetic structure and the behaviour of pollen vectors. Differences in pollen prepotency and the higher selfing rates observed at low floral densities in I. hexagona may have contributed to the observed patterns of hybrid seed formation. The analyses of family outcrossing rates provide important information on factors responsible for mating system variation and evolution.

Genetic variation associated with the natural hybridization of Iris fulva and I. hexagona was investigated to test for the occurrence of introgression. These species have been viewed as a classic example of the process of introgressive hybridization (Anderson, 1949). However, more recent studies have concluded that there has not been an exchange of genetic material between I. fulva and I. hexagona (Randolph et al., 1967). Our analysis has involved the examination of both allopatric and parapatric populations of I. fulva and I. hexagona with reference to diagnostic ribosomal DNA markers. The pattern of variation in the parapatric population indicates the presence of the repeated backcrossing necessary to the process of introgressive hybridization. Indeed, in the region of parapatry, we suggest that localized introgression of ribosomal sequences has occurred into both I. fulva and I. hexagona. Significantly, we have also detected the presence of the diagnostic ribosomal markers from each species in allopatric populations of the alternate species. Our findings suggest that not only is introgressive hybridization presently occurring in parapatry between I. fulva and I. hexagona, but that past hybridization between these species has resulted in introgression into areas of allopatry.

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