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17 Sentences With "choosiness"

How to use choosiness in a sentence? Find typical usage patterns (collocations)/phrases/context for "choosiness" and check conjugation/comparative form for "choosiness". Mastering all the usages of "choosiness" from sentence examples published by news publications.

Piece by piece, my framer has become intimate with me: my choosiness, my fondnesses, my dumb, entirely sincere urge to create remarkability.
Ms Fine uses studies of behaviour from across the animal kingdom to argue that neither sex has a monopoly on competitiveness, promiscuity, choosiness or parental care.
Why else am I willing to overlook the real problem — that even liberal Americans tend to approve of Muslims on a case-by-case basis, tend to like their Muslims as non-Muslim as possible, tend to think themselves entitled to this choosiness?
They found the following results: > 'Paradoxical' trait combinations yield particularly low payoffs: individuals > with low choosiness but high effort tend to get exploited by their co- > players; individuals with high choosiness but low effort waste their time > searching for better co-players, which are, however, unlikely to accept > them. The positive correlation between choosiness and cooperativeness leads > to a positive assortment between cooperative types – an essential feature of > all mechanisms that promote cooperation. The development of such cooperation requires variation in the degree of cooperation and choosiness, which the researchers attributed to genetic mutation and variation. McNamara et al.
Their fitness is lowered because they are ostracized by members of the flock. McNamara et al.McNamara, J., Z. Barta, L. Fromhage, and A. Houston. 2008. The coevolution of choosiness and cooperation.
Whether this is a result of male-male fighting or display, or of female choosiness differs depending on the species as the shape, size, and function of antlers vary between species.
Nature 451: 189-192. quantitatively analyzed this theory. Like Robert Axelrod, they created a computer program to simulate repeated interactions among individuals. The program involved players with two genetically determined traits, a "cooperative trait" and a "choosiness trait".
For mammals, the female has the slower reproduction rate. Males typically evolve either traits to help them fight other males or traits to impress females. Females typically evolve greater abilities to discern the qualities of males, such as choosiness in mating.
Clark and Hatfield found that 75% of men were willing to have sex with a female stranger when propositioned, compared to 0% of women. On the other hand, 50% of women agreed to a date with a male stranger. This suggests males seek short term relationships, while women show a strong preference for long- term relationships. However, these preferences (male promiscuity and female choosiness) can be explained in other ways.
The choice is most likely dependent on the search costs associated with finding a mate. When actively searching for a male, a female must spend her precious time and energy, which results in search costs, especially when she has a limited life span. As search costs increase, female choosiness for a mate decreases. For example, if a female's life span is shorter, she has a higher cost associated with searching for the ideal mate.
Two chapters on mammals precede those on humans. Darwin explained sexual selection as a combination of "female choosiness" and "direct competition between males". Antoinette Blackwell, one of the first women to write a critique of Darwin Darwin's theories of evolution by natural selection were used to try to show women's place in society was the result of nature. One of the first women to critique Darwin, Antoinette Brown Blackwell published The Sexes Throughout Nature in 1875.
In some species, such as the three-spined stickleback, the large investment in both nesting site and guarding of eggs by males limits the number of females a male can mate with. This introduces the ability for selection to favor male mate choice. Male mate choice is rarely studied or observed in many species but multiple studies have confirmed male mate choice within stickleback species. Males show a choosiness similar to females as to what female they are willing to court and mate.
For male mammals, which have a relatively fast reproduction rate, sexual selection leads to adaptations that help them compete for females. For female mammals, with a relatively slow reproduction rate, sexual selection leads to choosiness, which helps females select higher quality mates. Charles Darwin described both natural selection and sexual selection, but he relied on group selection to explain the evolution of self-sacrificing behavior. Group selection is a weak explanation because in any group the less self-sacrificing animals will be more likely to survive and the group will become less self- sacrificing.
Robert Trivers' theory of parental investment predicts that the sex making the largest investment in lactation, nurturing, and protecting offspring will be more discriminating in mating; and that the sex that invests less in offspring will compete via intrasexual selection for access to the higher-investing sex (see Bateman's principle). In species where both sexes invest highly in parental care, mutual choosiness is expected to arise. An example of this is seen in crested auklets, where parents share equal responsibility in incubating their single egg and raising the chick. In crested auklets, both sexes are ornamented.
For female mammals, with a relatively low maximal potential reproduction rate, sexual selection leads to choosiness, which helps females select higher quality mates. Charles Darwin described both natural selection and sexual selection, and he relied on group selection to explain the evolution of altruistic (self-sacrificing) behavior. But group selection was considered a weak explanation, because in any group the less altruistic individuals will be more likely to survive, and the group will become less self-sacrificing as a whole. In 1964, William D. Hamilton proposed inclusive fitness theory, emphasizing a gene-centered view of evolution.
These colors can be used to the males advantage in attracting a mate. In the species Habronattus pyrrithrix, the males who have faces that are red and non bright green legs are more likely to attract a mate than males who do not, indicating that females prefer males with those particular traits. Although females from the species, Hygrolycosa rubrofasciata, Schizocosa floridana and Schizocosa stridulans tend to be the choosier sex, it is not uncommon to observe males from different spider species such as the Zygiella x-notata and Latrodectus hesperus, to be choosy as well.Bel-Venner, M. C., Dray, S., Allainé, D., Menu, F. & Venner, S. Unexpected male choosiness for mates in a spider.
The effort to discover how costs can constrain an "honest" correlation between observable signals and unobservable qualities within signallers is built on strategic models of signalling games, with many simplifying assumptions. These models are most often applied to sexually selected signalling in diploid animals, but they rarely incorporate a fact about diploid sexual reproduction noted by the mathematical biologist Ronald Fisher in the early 20th century: if there are "preference genes" correlated with choosiness in females as well as "signal genes" correlated with display traits in males, choosier females should tend to mate with showier males. Over generations, showier sons should also carry genes associated with choosier daughters, and choosier daughters should also carry genes associated with showier sons. This can cause the evolutionary dynamic known as Fisherian runaway, in which males become ever showier.

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