scholarly journals Parental investment, mate choice, and mate quality.

1977 ◽  
Vol 74 (8) ◽  
pp. 3476-3479 ◽  
Author(s):  
N. Burley
2017 ◽  
Vol 190 (4) ◽  
pp. 534-546 ◽  
Author(s):  
Thomas R. Haaland ◽  
Jonathan Wright ◽  
Bram Kuijper ◽  
Irja I. Ratikainen

2009 ◽  
Vol 21 (1) ◽  
pp. 193-194 ◽  
Author(s):  
Klaudia Witte ◽  
Jean-Guy J. Godin

2020 ◽  
Vol 9 (8) ◽  
pp. 141
Author(s):  
Wendy Iredale ◽  
Keli Jenner ◽  
Mark Van Vugt ◽  
Tammy Dempster

One of the evolutionary adaptive benefits of altruism may be that it acts as an honest (reliable) signal of men’s mate quality. In this study, 285 female participants were shown one of three video scenarios in which a male target took £30 out of a cash machine (ATM) and gave either a lot (£30), a little (£1), or nothing to a homeless man. The participants rated the male target on his attractiveness, their short- and long-term mate preferences towards him, and the degree to which they thought he was likely to possess various parenting qualities. The results showed that, regardless of whether the man was described as rich or poor, participants rated him as being more attractive when he donated money, but only when the donation was costly (£30). In addition, altruism was shown to be important in long-term, but not short-term mate choice, and displays of altruism were associated with positive parenting qualities. It is argued that displays of altruism act as a reliable (honest) mate signal for a potential long-term parental partner.


2009 ◽  
Vol 20 (4) ◽  
pp. 908-911 ◽  
Author(s):  
Antonios Vakirtzis ◽  
S. Craig Roberts

2002 ◽  
Vol 357 (1419) ◽  
pp. 319-330 ◽  
Author(s):  
H. Kokko ◽  
R. A. Johnstone

Biases in the operational sex ratio (OSR) are seen as the fundamental reason behind differential competition for mates in the two sexes, and as a strong determinant behind differences in choosiness. This view has been challenged by Kokko and Monaghan, who argue that sex–specific parental investment, mortalities, mate–encounter rates and quality variation determine the mating system in a way that is not reducible to the OSR. We develop a game–theoretic model of choosiness, signalling and parental care, to examine (i) whether the results of Kokko and Monaghan remain robust when its simplifying assumptions are relaxed, (ii) how parental care coevolves with mating strategies and the OSR and (iii) why mutual mate choice is observed relatively rarely even when both sexes vary in quality. We find qualitative agreement with the simpler approach: parental investment is the primary determinant of sex roles instead of the OSR, and factors promoting choosiness are high species–specific mate–encounter rate, high sex–specific mate–encounter rate, high cost of breeding (parental investment), low cost of mate searching and highly variable quality of the opposite sex. The coevolution of parental care and mating strategies hinders mutual mate choice if one parent can compensate for reduced care by the other, but promotes it if offspring survival depends greatly on biparental care. We argue that the relative rarity of mutual mate choice is not due to biases in the OSR. Instead, we describe processes by which sexual strategies tend to diverge. This divergence is prevented, and mutual mate choice maintained, if synergistic benefits of biparental care render parental investment both high and not too different in the two sexes.


The Auk ◽  
1988 ◽  
Vol 105 (4) ◽  
pp. 672-680 ◽  
Author(s):  
David F. Gori

Abstract By removing young from the nests of competent females, I tested whether male Yellow-headed Blackbirds (Xanthocephalus xanthocephalus) could assess the parental competence of mates and adjust their parental investment accordingly. The purpose of this experimental reduction was to equalize the number of young in nests of parentally competent and incompetent females in order to control for the effect of offspring number on parental investment by males. Males had a greater probability of feeding at nests of competent-reduced females and they fed at a higher rate than they did at nests of incompetent females. The latter broods were fed only when nests belonging to competent females were unavailable. Males adjust their parental investment with mate quality independent of the number of young in nests. To explain this preference, I constructed functions to relate the amount of paternal investment (i.e. male feeding rate) to the number of young fledged from nests and the fledging mass of young. The latter are two components of male reproductive success and, therefore, estimates of the "return" on a male's parental investment. Male feeding had no effect on the number of young fledged from starvation-reduced or experimental nests. However, the fledging mass of young increased more when males helped competent females than when incompetent females were helped. Thus male preference for helping competent females may result because the return per unit of their investment is greater at these nests.


2016 ◽  
Vol 3 (3) ◽  
pp. 160027 ◽  
Author(s):  
Julien P. Renoult ◽  
Jeanne Bovet ◽  
Michel Raymond

Sexual ornaments are often assumed to be indicators of mate quality. Yet it remains poorly known how certain ornaments are chosen before any coevolutionary race makes them indicative. Perceptual biases have been proposed to play this role, but known biases are mostly restricted to a specific taxon, which precludes evaluating their general importance in sexual selection. Here we identify a potentially universal perceptual bias in mate choice. We used an algorithm that models the sparseness of the activity of simple cells in the primary visual cortex (or V1) of humans when coding images of female faces. Sparseness was found positively correlated with attractiveness as rated by men and explained up to 17% of variance in attractiveness. Because V1 is adapted to process signals from natural scenes, in general, not faces specifically, our results indicate that attractiveness for female faces is influenced by a visual bias. Sparseness and more generally efficient neural coding are ubiquitous, occurring in various animals and sensory modalities, suggesting that the influence of efficient coding on mate choice can be widespread in animals.


2020 ◽  
Author(s):  
Annemarie M. Hasnain

Both sexes choose mates based on qualities that will enhance offspring viability and quality. In some cases individuals are forced to reproduce with less desirable mates which has been shown to result in lower quality offspring. The Reproductive Compensation Hypothesis (RCH) predicts that parents who mate under constraint will increase their reproductive effort and investment in offspring to compensate for lowered offspring viability. Evidence for the RCH has been found in several animal species; however it has not been examined in humans. One possible type of mate choice constraint in humans is that of arranged marriage in which parents or others choose mates for individuals. In order to test the RCH, I examine whether there are differences in both partner traits between women in arranged marriages and those in self-choice marriages, and differences in parental investment between women in arranged and self-choice marriages using data from the Indonesian Family Life Survey. Except for husband’s education level, no differences were found in mate characteristics between the husbands of women in self-choice marriages and those in arranged marriages. Marriage type did not significantly correlate with parental investment except for number of live births. This correlation, however, was not in the predicated direction. Results show that women in self-choice marriages had more offspring (controlling for marriage duration) than woman in arranged marriages. It is possible that arranged marriage is not a true constraint on mate choice or that parental investment measures used in this study need to be more refined.


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