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Because the scales at which mating and density-dependent regulation occur are key factors for population dynamics and evolution [ 35], we here present a new model introducing important modifications: mating sites are independent from nesting sites, and population regulation may occur either within nesting sites (hereafter named HABITAT model) or at the level of the whole population (TOTAL model).
That might be because elevated mating sites are too dry or exposed to predators.
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Nonetheless, it remains possible that under natural conditions, cVA is used as a long distance co-attractant with food odors at mating sites while 9-tricosene is used as a short-range aggregation pheromone at food sites.
This segregation may be enhanced not only by different habitat use, but also by mating site fidelity, which has been previously demonstrated in A. gazella and other pinnipeds [ 29- 31], and may stabilise the population structure over time.
Generic criteria for specific mating and birthing sites are thought to include proximity to water and foraging grounds, safety from predators and shelter from inundation during high seas [ 11].
These food-rich sites are also popular places for meeting, mating, and rearing offspring.
Such sites are often used to find and attract potential mates.
The spatial distribution of mating type within study sites is often neglected in studies aiming at assessing the reproductive biology of fungal species.
Mice containing the two loxP sites were mated with the mouse line TgN Zp3-Cre Knw, expressing TgN Zp3-Cre Knwnasexpressinge conthel of the Zona pelluCrea 3 gene precombinaseive in oocytes [12].
At all doses tested, sperm motility, morphology, mating and pregnancy rates, and number of implantation sites were not affected.
The Case-Mate site, however, is a morass.
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