skip to main content

Title: Dehydrated males are less likely to dive into the mating pool
Abstract

The hydration state of animals vying for reproductive success may have implications for the tempo and mode of sexual selection, which may be salient in populations that experience increasing environmental fluctuations in water availability. Using red-sided garter snakes as a model system, we tested the effect of water supplementation on courtship, mating behavior, and copulatory plug (CP) production during a drought year. Over 3 days of mating trials, water-supplemented males (WET males, n = 45) outperformed a control group that was not supplemented with water (DRY males, n = 45). Over 70% of WET males mated but just 33% of DRY males did so. As a group, WET males mated 79 times versus 28 times by DRY males. On the last day of mating trials, over 70% of WET males were still courting, with 19 of them mating, whereas less than 25% of DRY males were courting and only one mated. CP deposition accounted for 4–6% of the mass lost by mating males, but hydration did not affect CP mass or water content. These findings suggest that, in years of low water availability, the number of courting males and the intensity of their courtship declines, thereby affecting sexual selection more » and conflict, at least within that year.

« less
Authors:
; ; ;
Publication Date:
NSF-PAR ID:
10388760
Journal Name:
Behavioral Ecology
Volume:
33
Issue:
2
Page Range or eLocation-ID:
p. 436-445
ISSN:
1045-2249
Publisher:
Oxford University Press
Sponsoring Org:
National Science Foundation
More Like this
  1. Abstract

    Animals often communicate in complex, heterogeneous environments, leading to hypothesized selection for increased detectability or discriminability in signaling traits. The extent to which secondary sexual ornaments have evolved to overcome the challenges of signaling in complex environments, however, remains understudied, especially in comparison to their role as indicator traits. This study tested the hypothesis that the condition-dependent secondary sexual ornamentation in the wolf spider Rabidosa rabida functions to increase detectability/discriminability in visually complex environments. We predicted that male ornamentation would interact with the complexity of the signaling environment to affect male mating success. In particular, we expected ornaments to confer a greater mating advantage when males courted in visually complex environments. To test this, we artificially manipulated male foreleg ornamentation (present/absent) and ran repeated-measures mating trials across laboratory microcosms that represented simple versus complex visual signaling environments. Microcosm visual complexity differed in their background pattern, grass stem color, and grass stem placement. We found that ornamented males mated more often and more quickly than unornamented males across both environments, but we found no support for an ornament-by-environment interaction. Male courtship rate, however, did interact with the signaling environment. Despite achieving the same level of mating success across signaling environments,more »ornamented males courted less rapidly in complex versus simple environments, although environmental complexity had no influence on unornamented male courtship rates. Our results suggest that the visual complexity of the signaling environment influences the interactive influence of ornamentation and dynamic visual courtship on female mate choice.

    « less
  2. Abstract Background

    Ever since Darwin, evolutionary biologists have studied sexual selection driving differences in appearance and behaviour between males and females. An unchallenged paradigm in such studies is that one sex (usually the male) signals its quality as a mate to the other sex (usually the female), who is choosy in accepting a partner. Here, we hypothesize that in polygamous species these roles change dynamically with the mating status of males and females, depending on direct reproductive costs and benefits of multiple matings, and on sperm competition. We test this hypothesis by assessing fitness costs and benefits of multiple matings in both males and females in a polygamous moth species, as in moths not males but females are the signalers and males are the responders.

    Results

    We found that multiple matings confer fitness costs and benefits for both sexes. Specifically, the number of matings did not affect the longevity of males or females, but only 67% of the males and 14% of the females mated successfully in all five nights. In addition, the female’s reproductive output increased with multiple matings, although when paired with a new virgin male every night, more than 3 matings decreased her reproductive output, so that the Batemanmore »gradient for females fit a quadratic model better than a linear model. The male’s reproductive success was positively affected by the number of matings and a linear regression line best fit the data. Simulations of the effect of sperm competition showed that increasing last-male paternity increases the steepness of the male Bateman gradient and thus the male’s relative fitness gain from additional mating. Irrespective of last-male paternity value, the female Bateman gradient is steeper than the male one for up to three matings.

    Conclusion

    Our results suggest that choosiness in moths may well change throughout the mating season, with males being more choosy early in the season and females being more choosy after having mated at least three times. This life-history perspective on the costs and benefits of multiple matings for both sexes sheds new light on sexual selection forces acting on sexual signals and responses.

    « less
  3. Synopsis Sound production in tiger moths (Erebidae: Arctiinae) plays a role in natural selection. Some species use tymbal sounds as jamming signals avoiding bat predation. High duty cycle signals have the greatest efficacy in this regard. Tiger moth sounds can also be used for intraspecific communication. Little is known about the role of sound in the mating behavior of jamming species or the signal preferences underlying mate choice. We recorded sound production during the courtship of two high duty cycle arctiines, Bertholdia trigona and Carales arizonensis. We characterized variation in their acoustic signals, measured female preference for male signals that vary in duty cycle, and performed female choice experiments to determine the effect of male duty cycle on the acceptance of male mates. Although both species produced sound during courtship, the role of acoustic communication appears different between the species. Bertholdia trigona was acoustically active in all intraspecific interactions. Females preferred and ultimately mated with males that produced higher duty cycles. Muted males were never chosen. In C. arizonensis however, sound emissions were limited during courtship and in some successful matings no sound was detected. Muted and clicking males were equally successful in female mate-choice experiments, indicating that acoustic communicationmore »is not essential for mating in C. arizonensis. Our results suggest that in B. trigona natural and sexual selection may work in parallel, to favor higher duty cycle clicking.« less
  4. Abstract

    Animal signals experience selection for detectability, which is determined in large part by the signal transmission properties of the habitat. Understanding the ecological context in which communication takes place is therefore critical to understanding selection on the form of communication signals. In order to determine the influence of environmental heterogeneity on signal transmission, we focus on a wolf spider species native to central Florida, Schizocosa floridana, in which males court females using a substrate-borne vibratory song. We test the hypothesis that S. floridana is a substrate specialist by 1) assessing substrate use by females and males in the field, 2) quantifying substrate-specific vibratory signal transmission in the laboratory, and 3) determining substrate-specific mating success in the laboratory. We predict a priori that 1) S. floridana restricts its signaling to oak litter, 2) oak litter best transmits their vibratory signal, and 3) S. floridana mates most readily on oak litter. We find that S. floridana is almost exclusively found on oak litter, which was found to attenuate vibratory courtship signals the least. Spiders mated with equal frequency on oak and pine, but did not mate at all on sand. Additionally, we describe how S. floridana song contains a novel component,more »chirps, which attenuate more strongly than its other display components on pine and sand, but not on oak, suggesting that the ways in which the environment relaxes restrictions on signal form may be as important as the ways in which it imposes them.

    « less
  5. BACKGROUND Charles Darwin’s  Descent of Man, and Selection in Relation to Sex  tackled the two main controversies arising from the Origin of Species:  the evolution of humans from animal ancestors and the evolution of sexual ornaments. Most of the book focuses on the latter, Darwin’s theory of sexual selection. Research since supports his conjecture that songs, perfumes, and intricate dances evolve because they help secure mating partners. Evidence is overwhelming for a primary role of both male and female mate choice in sexual selection—not only through premating courtship but also through intimate interactions during and long after mating. But what makes one prospective mate more enticing than another? Darwin, shaped by misogyny and sexual prudery, invoked a “taste for the beautiful” without speculating on the origin of the “taste.” How to explain when the “final marriage ceremony” is between two rams? What of oral sex in bats, cloacal rubbing in bonobos, or the sexual spectrum in humans, all observable in Darwin’s time? By explaining desire through the lens of those male traits that caught his eyes and those of his gender and culture, Darwin elided these data in his theory of sexual evolution. Work since Darwin has focused on howmore »traits and preferences coevolve. Preferences can evolve even if attractive signals only predict offspring attractiveness, but most attention has gone to the intuitive but tenuous premise that mating with gorgeous partners yields vigorous offspring. By focusing on those aspects of mating preferences that coevolve with male traits, many of Darwin’s influential followers have followed the same narrow path. The sexual selection debate in the 1980s was framed as “good genes versus runaway”: Do preferences coevolve with traits because traits predict genetic benefits, or simply because they are beautiful? To the broader world this is still the conversation. ADVANCES Even as they evolve toward ever-more-beautiful signals and healthier offspring, mate-choice mechanisms and courter traits are locked in an arms race of coercion and resistance, persuasion and skepticism. Traits favored by sexual selection often do so at the expense of chooser fitness, creating sexual conflict. Choosers then evolve preferences in response to the costs imposed by courters. Often, though, the current traits of courters tell us little about how preferences arise. Sensory systems are often tuned to nonsexual cues like food, favoring mating signals resembling those cues. And preferences can emerge simply from selection on choosing conspecifics. Sexual selection can therefore arise from chooser biases that have nothing to do with ornaments. Choice may occur before mating, as Darwin emphasized, but individuals mate multiple times and bias fertilization and offspring care toward favored partners. Mate choice can thus occur in myriad ways after mating, through behavioral, morphological, and physiological mechanisms. Like other biological traits, mating preferences vary among individuals and species along multiple dimensions. Some of this is likely adaptive, as different individuals will have different optimal mates. Indeed, mate choice may be more about choosing compatible partners than picking the “best” mate in the absolute sense. Compatibility-based choice can drive or reinforce genetic divergence and lead to speciation. The mechanisms underlying the “taste for the beautiful” determine whether mate choice accelerates or inhibits reproductive isolation. If preferences are learned from parents, or covary with ecological differences like the sensory environment, then choice can promote genetic divergence. If everyone shares preferences for attractive ornaments, then choice promotes gene flow between lineages. OUTLOOK Two major trends continue to shift the emphasis away from male “beauty” and toward how and why individuals make sexual choices. The first integrates neuroscience, genomics, and physiology. We need not limit ourselves to the feathers and dances that dazzled Darwin, which gives us a vastly richer picture of mate choice. The second is that despite persistent structural inequities in academia, a broader range of people study a broader range of questions. This new focus confirms Darwin’s insight that mate choice makes a primary contribution to sexual selection, but suggests that sexual selection is often tangential to mate choice. This conclusion challenges a persistent belief with sinister roots, whereby mate choice is all about male ornaments. Under this view, females evolve to prefer handsome males who provide healthy offspring, or alternatively, to express flighty whims for arbitrary traits. But mate-choice mechanisms also evolve for a host of other reasons Understanding mate choice mechanisms is key to understanding how sexual decisions underlie speciation and adaptation to environmental change. New theory and technology allow us to explicitly connect decision-making mechanisms with their evolutionary consequences. A century and a half after Darwin, we can shift our focus to females and males as choosers, rather than the gaudy by-products of mate choice. Mate choice mechanisms across domains of life. Sensory periphery for stimulus detection (yellow), brain for perceptual integration and evaluation (orange), and reproductive structures for postmating choice among pollen or sperm (teal). ILLUSTRATION: KELLIE HOLOSKI/ SCIENCE« less