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Species of the former mating system are called heterothallic, and of the latter homothallic.
Correlations between genome size and generation time and mating system are also widely discussed but are less clear.
These effects of the mating system are expected to occur irrespective of population structure and hence add to the effects of dispersal rate and deme size predicted here.
The potential for reproductive assurance is therefore likely to be overestimated if the pollination parameters and the actual mating system are not assessed together with lifetime ID.
Even if the selective effects of the mating system are separated from its purely combinational effects, as was possible in the one-locus model, recombination apparently introduces dynamical forces which become dominant for compensating forms of selection and combination.
Home range, group size and mating system are all strongly phylogenetically conserved in gibbons, meaning that more closely related gibbon species resemble each other in terms of these behavioural and ecological traits more than expected by chance.
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This had not been tested in previous studies because accurate quantifications of mating system were missing.
Intraspecific variation in mating system was found in all four species.
However, mating system was not quantified precisely in these studies [ 2- 4, 7].
For example, mating system is likely to confer unequal probabilities of speciation and extinction.
Similarly, no difference in relative ovary length among females differing in mating system was observed.
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