Sentence examples for mating frequencies were from inspiring English sources

Observed and expected mating frequencies were compared with a χ2-test.

Observations of morph mating frequencies were done between 2007 and 2009 at seven populations in Spain (Laxe, Louro and Doniños), Italy (Canale Reale) and the Netherlands (Hilversum, Koudekerke and Zouweboezem).

Though the field and molecular data on mating frequencies were consistent, we noted that the molecular data yielded more sensitive measures on mating frequencies, allowing the detection of smaller differences in mating numbers than classical field observations.

Our field data showed that although morph frequencies varied widely over space and time (androchrome females ranged from 15-94% per population), morph mating frequencies were in all populations (except Laxe and Louro) lower for the androchrome females than for the gynochrome females (Table  1).

Mating frequencies were the number of each mature morph in copula divided by the total number of mature morphs in copula (Table  1).

For example, in experiments using mitotracker to visualize transferred sperm, we also observed that mating frequencies were similar for wild-type and comp-1 males.

Of note, other independent measurements of mating frequency were consistent with comp-1 males having high mating frequencies that are similar to those of wild-type animals.

As a result, mating frequency is significantly reduced.

It remains to be assessed experimentally whether mating frequency is affected by stc KG01230.

Large female body size has great advantages in fecundity and mating behavior (A. Walzer & P. Schausberger, unpubl. data) and female lifetime mating frequencies are lower than those of males.

This is realized by Substitution of "allele" for "type" and considering the formation of a zygote as a mating event, the conditional mating frequencies are given by ½ b lk / b k for l ≠ k and by b kk /b k for l = k.