scholarly journals The evolution of female ornaments and weaponry: social selection, sexual selection and ecological competition

2012 ◽  
Vol 367 (1600) ◽  
pp. 2274-2293 ◽  
Author(s):  
Joseph A. Tobias ◽  
Robert Montgomerie ◽  
Bruce E. Lyon

Ornaments, weapons and aggressive behaviours may evolve in female animals by mate choice and intrasexual competition for mating opportunities—the standard forms of sexual selection in males. However, a growing body of evidence suggests that selection tends to operate in different ways in males and females, with female traits more often mediating competition for ecological resources, rather than mate acquisition. Two main solutions have been proposed to accommodate this disparity. One is to expand the concept of sexual selection to include all mechanisms related to fecundity; another is to adopt an alternative conceptual framework—the theory of social selection—in which sexual selection is one component of a more general form of selection resulting from all social interactions. In this study, we summarize the history of the debate about female ornaments and weapons, and discuss potential resolutions. We review the components of fitness driving ornamentation in a wide range of systems, and show that selection often falls outside the limits of traditional sexual selection theory, particularly in females. We conclude that the evolution of these traits in both sexes is best understood within the unifying framework of social selection.

2015 ◽  
Vol 282 (1816) ◽  
pp. 20151987 ◽  
Author(s):  
Ulrika Candolin ◽  
Iina Tukiainen

Extravagant male ornaments expressed during reproduction are almost invariably assumed to be sexually selected and evolve through competition for mating opportunities. Yet in species where male reproductive success depends on the defence of offspring, male ornaments could also evolve through social competition for offspring survival. However, in contrast to female ornaments, this possibility has received little attention in males. We show that a male ornament that is traditionally assumed to be sexually selected—the red nuptial coloration of the three-spined stickleback—is under stronger selection for offspring survival than for mating success. Males express most coloration during parenting, when they no longer attract females, and the colour correlates with nest retention and hatching success but not with attractiveness to females. This contradicts earlier assumptions and suggests that social selection for offspring survival rather than for sexual selection for mating success is the main mechanism maintaining the ornament in the population. These results suggest that we should consider other forms of social selection beyond sexual selection when seeking to explain the function and evolution of male ornaments. An incorrect assignment of selection pressures could hamper our understanding of evolution.


Author(s):  
Tatiana Sella Tunis ◽  
Israel Hershkovitz ◽  
Hila May ◽  
Alexander Dan Vardimon ◽  
Rachel Sarig ◽  
...  

The chin is a unique anatomical landmark of modern humans. Its size and shape play an important role from the esthetic perspective. However, disagreement exists in the dental and anthropological literature regarding the sex differences in chin and symphysis morphometrics. The “sexual selection” theory is presented as a possible reason for chin formation in our species; however, many other contradictory theories also exist. This study’s aims were therefore to determine how chin and symphysis size and shape vary with sex, and to discuss “sexual selection” theory as a reason for its formation. Head and neck computed tomography (CT) scans of 419 adults were utilized to measure chin and symphysis sizes and shapes. The chin and symphysis measures were compared between the sexes using an independent-samples t-test, a Mann–Whitney test, and the F-statistic. The chin width was significantly greater in males than in females (p < 0.001), whereas the chin height, area, and size index were significantly greater in females (p < 0.001). Symphysis measures did not differ significantly between the sexes. Size accounted for 2–14% of the chin variance and between 24–33% of the symphysis variance. Overall, the chin was found to be a more heterogeneous anatomical structure than the symphysis, as well as more sexually dimorphic.


Evolution ◽  
1986 ◽  
Vol 40 (2) ◽  
pp. 446
Author(s):  
Randy Thornhill ◽  
Carl Jay Bajema

2012 ◽  
Vol 367 (1600) ◽  
pp. 2266-2273 ◽  
Author(s):  
Bruce E. Lyon ◽  
Robert Montgomerie

Social selection influences the evolution of weapons, ornaments and behaviour in both males and females. Thus, social interactions in both sexual and non-sexual contexts can have a powerful influence on the evolution of traits that would otherwise appear to be detrimental to survival. Although clearly outlined by West-Eberhard in the early 1980s, the idea that social selection is a comprehensive framework for the study of ornaments and weapons has largely been ignored. In West-Eberhard's view, sexual selection is a form of social selection—a concept supported by several lines of evidence. Darwin's distinction between natural and sexual selection has been useful, but recent confusion about the limits of sexual selection suggests that some traits are not easily categorized as naturally or sexually selected. Because social selection theory has much to offer the current debates about both sexual selection and reproductive competition in females, it is sometimes viewed, narrowly, to be most useful when considering female roles. However, social selection theory encompasses much more than female reproductive competition. Our goal here was to provide that broader perspective.


Author(s):  
Ingo Schlupp

When Darwin first proposed sexual selection theory he suggested two mechanisms: competition among males and choice by females. There is no doubt that these mechanisms are immensely important, but their mirror images have been largely underappreciated so far. In fact, males choose as well and females compete. Males choose based on female quality, often selecting mating partners that are more fecund. But male choice is also associated with changes in the sex ratio of a population and males can be choosy when they are rare. Furthermore, males sometimes invest heavily into reproduction and that too can be associated with male choice. That females compete with another, although less often with open aggression, is another understudied phenomenon. Finally, we now know that females are often ornamented, but are these ornaments under sexual selection by males? This book tries to review what we know and point to what we don’t know while pointing out the connections between male mate choice and female competition for a more complete view of sexual selection.


Author(s):  
Leigh W. Simmons

The idea that males and females often look, sound, smell, and behave differently is uncontroversial. Where those differences came from, however, and what role they play in various species—including humans—is not. ‘Darwin’s other big idea’ outlines Charles Darwin’s sexual selection theory: differential reproduction based on sexual competition, whether between the members of one sex for access to the other, or by selection of particular mating partners. Differences in reproductive parts directly involved in sperm or egg production—primary sexual characteristics—were relatively easy to explain. The other kinds of sexual differences, he proposed, could evolve in one of two ways: male–male competition resulting in weapons, or female choice resulting in ornaments, but this was highly controversial.


1987 ◽  
Vol 35 (2) ◽  
pp. 123 ◽  
Author(s):  
D Cook

Sexual dimorphism in horned beetles reflects a history of different selection pressures operating on males and females. A multivariate morphometric analysis was carried out on two scarabaeine dung beetles, Onthophagus binodis Thunberg and O. ferox Harold. There is clear structural polymorphism within O. binodis; horned males, females and hornless males were separated on the basis of body shape. Sexual dimorphism within O. ferox was established; sexes were separated according to the size of pronotal and cephalic horns. The effect of differential selection is discussed within the context of sexual selection.


2021 ◽  
Author(s):  
Salom&eacute Fromonteil ◽  
Lennart Winkler ◽  
Lucas Marie-Orleach ◽  
Tim Janicke

The pioneers of sexual selection theory proposed that males are generally "eager" whereas females are rather "coy" with respect to mating. This male-centred perspective on sexual selection continues to permeate our perception of sex differences across disciplines. Despite an increased awareness that females also compete for mating partners, we still tend to consider sexual selection in females a rare peculiarity. Here we present meta-analytic evidence from 72 species across a broad range of animal taxa to show that sexual selection in females is widespread and should be considered the norm rather than the exception. Thereby, our results extend our general understanding of sexual reproduction and may contribute to a more balanced perspective of how sexual selection operates in both males and females.


2021 ◽  
Vol 17 (9) ◽  
pp. 20210283
Author(s):  
América Hernández ◽  
Margarita Martínez-Gómez ◽  
René Beamonte-Barrientos ◽  
Bibiana Montoya

Colourful traits in females are suggested to have evolved and be maintained by sexual selection. Although several studies have evaluated this idea, support is still equivocal. Evidence has been compiled in reviews, and a handful of quantitative syntheses has explored cumulative support for the link between condition and specific colour traits in males and females. However, understanding the potential function of females' colourful traits in sexual communication has not been the primary focus of any of those previous studies. Here, using a meta-analytic approach, we find that evidence from empirical studies in birds supports the idea that colourful female ornaments are positively associated with residual mass and immune response, clutch size and male-mate preferences. Hence, colourful traits in female birds likely evolved and are maintained by sexual selection as condition-dependent signals.


2019 ◽  
Vol 4 ◽  
pp. 103-114
Author(s):  
Rucha Karkarey ◽  
Amod Zambre ◽  
Kavita Isvaran ◽  
Rohan Arthur

Historically unfished, high-density spawning aggregations are vanishingly uncommon. Behavioural observations from such aggregations are rare, and may be sometimes novel and unexpected. Given the weight of evidence required to document spawning aggregations, how can we best report rare and unusual behavioural variations in spawning populations? Based on two years of in-water observations of a high-density spawning aggregation of the squaretail grouper in the Lakshadweep Archipelago, we described a previously unreported male alternative reproductive tactic (ART) and an inverse size assortment with large males courting several small females that shoaled mid-water (https://doi.org/10.1186/s12898-017-0120-5). In critiquing our manuscript, it has been suggested that our observations, methodologies and interpretation are inadequate, flawed, and do not fit within currently accepted theory (https://doi.org/10.1186/s12898-018-0206-8). While offering a detailed counter of the main methodological and theoretical criticisms we question how best to document and interpret novel behaviours in poorly known systems. Reporting novelty itself can hardly be the basis of criticism. Our report relied on direct in-water observations, conducted at peak densities over two spawning years. The critique ignores this, choosing instead to focus on a supplementary video which was not the basis of our conclusions. Like other researchers working on this species, we did not directly observe mating, but report courtship as a well-established proxy used across mating systems studies. Apart from these methodological concerns, the authors suggest that there is no theoretical support for our observations. However, sexual selection theory provides well-established frameworks showing that, at very high mating densities, a variety of tactics can emerge, that often vary considerably between populations and locations. In our original paper, we use this broader theory of sexual selection together with detailed behavioural data to propose plausible evolutionary explanations that bear testing in these novel, high-density systems. We agree with the authors that novel observations should be scrutinised carefully as they can challenge our current understanding of the range of behaviours populations display and serve as a springboard for theoretical advancement. Given their rarity, these observations should be evaluated against the rigour of their documentation and the transparency of their reporting. In this context, we hope our carefully documented observations serve as a useful addition to the fascinating and complex natural history of species like the squaretail grouper.


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