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We conclude that there is likely a sexual conflict over mating frequency in the high-density species (L. saxatilis) owing to females most likely being less sperm-limited in this species.
Furthermore, we hypothesize that the difference in male behaviour between L. littorea and L. saxatilis is a consequence of a potentially more pronounced sexual conflict over mating frequency in the latter species, owing to its much higher density and prolonged mating-season.
Infection with N. whitei has been found to decrease mating frequency in T. castaneum[ 15].
We estimated that <1% of the segregants were h + cells, based on quantitations of mating frequency in the mutant pool.
The strongest evidence for this hypothesis come from experimental manipulation of mating frequency in bees [ 95, 96].
First, we measured the correlation of natural sperm depletion and mating frequency in N2 and HW hermaphrodites.
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Previous studies investigating morph and morph specific mating frequencies in the damselfly Ischnura elegans suggest that male mating harassment may promote the maintenance of this sexual mating polymorphism in females through density- and frequency-dependent processes [ 19- 22].
Here, we study mating frequencies in the wild and experimentally assess innate male preferences and learning of male preferences in I. elegans to investigate the extent of ontogenetic changes in male mate preferences during development.
Additional file 1: Additional analyses outlining module characteristics, mating frequency data in base population and GO analyses for each module.
Hence, a sexual conflict over mating frequency may evolve in species where females are forced to engage in costly matings.
With the caveat that these strains were collected over several decades and maintained in laboratory environments, this pattern of behavioral variation suggests that hermaphrodite mating frequency likely varies in natural populations.
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