scholarly journals Polyandry and alternative mating tactics

2013 ◽  
Vol 368 (1613) ◽  
pp. 20120045 ◽  
Author(s):  
Bryan D. Neff ◽  
Erik I. Svensson

Many species in the animal kingdom are characterized by alternative mating tactics (AMTs) within a sex. In males, such tactics include mate guarding versus sneaking behaviours, or territorial versus female mimicry. Although AMTs can occur in either sex, they have been most commonly described in males. This sex bias may, in part, reflect the increased opportunity for sexual selection that typically exists in males, which can result in a higher probability that AMTs evolve in that sex. Consequently, females and polyandry can play a pivotal role in governing the reproductive success associated with male AMTs and in the evolutionary dynamics of the tactics. In this review, we discuss polyandry and the evolution of AMTs. First, we define AMTs and review game theoretical and quantitative genetic approaches used to model their evolution. Second, we review several examples of AMTs, highlighting the roles that genes and environment play in phenotype expression and development of the tactics, as well as empirical approaches to differentiating among the mechanisms. Third, ecological and genetic constraints to the evolution of AMTs are discussed. Fourth, we speculate on why female AMTs are less reported on in the literature than male tactics. Fifth, we examine the effects of AMTs on breeding outcomes and female fitness, and as a source, and possibly also a consequence, of sexual conflict. We conclude by suggesting a new model for the evolution of AMTs that incorporates both environmental and genetic effects, and discuss some future avenues of research.

2017 ◽  
Author(s):  
Gavan M Cooke ◽  
Claire Johnson ◽  
Tony Reed ◽  
Andrew C Jackson

AbstractAlternative mating tactics (AMTs) are common in the animal kingdom, yet much work remains before their evolution and role in driving sexual selection is fully understood. Utilizing features of citizen science, we present compelling evidence that a third species in the cuttlefish genusSepia(Cephalopoda) possess males who use sneaky mating and female mimicry as alternative strategies to conspicuous signalling and fighting. We also present new evidence of large aggregations (n~30) in this species that possibly drive alternative mating strategies. Lastly, we provide footage of an opportunistic sneaky copulation in this species. We believe that alternative mating tactics may be more common in this genus than previously recorded (based on observations presented here and a search of the literature for similar life history, environmental and behavioural factors found in other species within theSepiagenus), and as much of their captive husbandry is well known, they could an ideal system for studying the evolution of alternative reproductive strategies.


Behaviour ◽  
2010 ◽  
Vol 147 (11) ◽  
pp. 1443-1460 ◽  
Author(s):  
Molly Morris ◽  
Abby Darrah ◽  
Oscar Rios-Cardenas

AbstractFemale mimicry is commonly considered in the context of alternative mating tactics as mimics can avoid male–male competition to gain increased access to females. We describe a case where one of the benefits to being a female mimic could be the increase in size of a sexually selected trait that should eventually decrease the mimics' ability to fool males. In the swordtail fish Xiphophorus nezahualcoyotl, a small percentage of males have a permanent pigment pattern known as 'false brood spot' (FBS), express a horizontal bar pigment pattern common for females, and yet have longer swords (a sexually selected trait) for their body size. FBS males did not use more 'coercive' behaviours in the field, and females do not appear to distinguish between males based on whether or not they have FBS in the laboratory. However, in the field males with FBS were chased less by other males, spent significantly more time feeding, and those that expressed the horizontal bar had greater access to females. We suggest that FBS males with swords can still fool other males into thinking they are females because the true brood spot remains informative as long as the frequency of FBS males (mimics) remains low.


2018 ◽  
Vol 137 ◽  
pp. 75-82 ◽  
Author(s):  
Anna Maria Skwierzyńska ◽  
Agata Plesnar-Bielak ◽  
Michał Kolasa ◽  
Jacek Radwan

1996 ◽  
Vol 7 (3) ◽  
pp. 334-340 ◽  
Author(s):  
Paula Stockley ◽  
Jeremy B. Searle ◽  
David W. Macdonald ◽  
Catherine S. Jones

2008 ◽  
Vol 20 (1) ◽  
pp. 153-159 ◽  
Author(s):  
Craig A. Walling ◽  
Clare E. Stamper ◽  
Claire L. Salisbury ◽  
Allen J. Moore

2020 ◽  
pp. 27-62
Author(s):  
John M. McNamara ◽  
Olof Leimar

Standard examples in biological game theory are introduced. The degree of cooperation at evolutionary stability is analysed in models that deal with situations such as the Prisoner’s Dilemma, the Tragedy of the Commons and the conflict of interest between parents over care of their common young. Several models of aggressive interactions are treated in this book. In this chapter the Hawk–Dove game, which is the simplest of these models, is analysed. Further models in the chapter deal with the situation in which individuals vary in their fighting ability and the situation in which information about the opponent is available before an individual decides whether to be aggressive. The problem of the allocation of resources to sons versus daughters has played a central role in biological game theory. This chapter introduces the basic theory, as well as a model in which the environmental temperature affects the development of the sexes differentially, so that at evolutionary stability the sex of offspring is determined by this temperature. Coordination games, alternative mating tactics, dispersal to avoid kin competition, and the idea that signals can evolve from cues are also introduced.


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