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Analyses of mate recognition between individual thrips of the Australian Bryophyllum population and a South African horticultural population, using reciprocal cross-mating tests, indicate that mating between the two host-associated populations occurs at a much lower frequency than mating within each of the two populations, even in confinement (Rafter and Walter 2013b).
In the latter scenario, lack of contact zones (and thus mating) between the resulting allopatric fragments is likely to lead to accumulation of colony (or fragment-) specific mutations and CHC compounds.
The frequency of mating between the three genotypes depends on their (i) frequencies in the population and (ii) the relative preference the males gain from females during mating.
Like Clark [ 5, 11], we found two groups of non-interbreeding individuals; however, we observed a few instances of mating between the groups.
These differences between the thresholds are largely due to the differences in the chances of mating between the wild-type adult females and the introduced males at the time of introduction.
We have demonstrated that the closely related species S. cerevisiae and S. paradoxus show lower levels of interspecific hybridisation than would be expected if mating between the two were random with respect to species.
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Confinement within the ascus is thought to enforce mating between products of the same meiotic division, minimizing outcrossing in this stage of the life cycle.
A possible alternative, mating between isolates of the same mating type, has been demonstrated [12].
Despite their significant divergence, mating between strains of the two varieties can occur.
The progeny from mating between homozygous mice still exhibits the ∼45% mortality rate within the first 3 days.
Such a barrier can evolve readily in the laboratory under artificial selection against mating between genetically marked strains of the same species [ 16].
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