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We also expected that mating probabilities were similar between treatment 2 and control.
When mating probabilities were estimated separately for intra and inter morphotypes (2p: a = d and b = c) this led to a significant improvement in fit of the model (G = 119.73, d.f. = 1 and p < 0.0001).
Thus, in the culicine case, when worm mating probabilities were not included and where the L3 uptake and development function shows only limiting behaviour, the results show that the system gives rise to just one threshold - a vector biting rate below which the only stable equilibrium was at the zero parasite level (Fig. 2A).
Mating probabilities were estimated using likelihood as described in the text, with upper and lower confidence intervals shown.
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Second, mating probability is under full female control, excluding systems in which females accept matings due to sexual harassment.
It is far from certain that mating probabilities will be the same at different genotype ratios and densities [ 30].
For each scenario and various values of mating probability for diploid males, 1000 simulations were run, each across 100 generations.
Mate-finding probability was unaffected by population density, suggesting the absence of mate-finding Allee effect, and population growth rate increased with decreasing density, suggesting negative density-dependence.
These probabilities are historical.
Logical probabilities are admissible.
Alternatively, in systems where females have full control over mating probability and mating partners are chosen randomly, theoretical work predicts that mating rates should remain unresponsive to variation in population density [ 11].
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