Population Structure Mediates Sexual Conflict in Water Striders

Science ◽  
2009 ◽  
Vol 326 (5954) ◽  
pp. 816-816 ◽  
Author(s):  
O. T. Eldakar ◽  
M. J. Dlugos ◽  
J. W. Pepper ◽  
D. S. Wilson
Behaviour ◽  
2010 ◽  
Vol 147 (12) ◽  
pp. 1615-1631 ◽  
Author(s):  
David Sloan Wilson ◽  
John Pepper ◽  
Michael Dlugos ◽  
Omar Tonsi Eldakar ◽  
Galen Holt

2019 ◽  
pp. 295-320
Author(s):  
Adolfo Cordero-Rivera ◽  
Anais Rivas-Torres

2018 ◽  
Author(s):  
Antonin Jean Johan Crumière ◽  
David Armisén ◽  
Aïdamalia Vargas-Lowman ◽  
Martha Kubarakos ◽  
Felipe Ferraz Figueiredo Moreira ◽  
...  

AbstractSexual conflict may result in the escalating coevolution of sexually antagonistic traits. However, our understanding of the evolutionary dynamics of antagonistic traits and their role in association with sex-specific escalation remains limited. Here we study sexually antagonistic coevolution in a genus of water striders called Rhagovelia. We identified a set of male grasping traits and female anti-grasping traits used during pre-mating struggles and show that natural variation of these traits is associated with variation in mating performance in the direction expected for antagonistic co-evolution. Phylogenetic mapping detected signals of escalation of these sexually antagonistic traits suggesting an ongoing arms race. Moreover, their escalation appears to be constrained by a trade-off with dispersal through flight in both sexes. Altogether our results highlight how sexual interactions may have shaped sex-specific antagonistic traits and how constraints imposed by natural selection may have influenced their evolution.


2018 ◽  
Vol 373 (1757) ◽  
pp. 20170418 ◽  
Author(s):  
Jennifer C. Perry ◽  
Locke Rowe

Sexual conflict can lead to rapid and continuous coevolution between females and males, without any inputs from varying ecology. Yet both the degree of conflict and selection on antagonistic traits are known to be sensitive to local ecological conditions. This leads to the longstanding question: to what extent does variation in ecological context drive sexually antagonistic coevolution? In water striders, there is much information about the impacts of ecological factors on conflict, and about patterns of antagonistic coevolution. However, the connection between the two is poorly understood. Here, we first review the multiple ways in which ecological context might affect the coevolutionary trajectory of the sexes. We then review ecological and coevolutionary patterns in water striders, and connections between them, in light of theory and new data. Our analysis suggests that ecological variation does impact observed patterns of antagonistic coevolution, but highlights significant uncertainty due to the multiple pathways by which ecological factors can influence conflict and its evolutionary outcome. To the extent that water striders are a reasonable reflection of other systems, this observation serves as both an opportunity and a warning: there is much to learn, but gaining insight may be a daunting process in many systems. This article is part of the theme issue ‘Linking local adaptation with the evolution of sex differences'.


2019 ◽  
Vol 15 (2) ◽  
pp. 20180720 ◽  
Author(s):  
Antonin Jean Johan Crumière ◽  
Abderrahman Khila

Sexual conflict occurs when traits favoured in one sex impose fitness costs on the other sex. In the case of sexual conflict over mating rate, the sexes often undergo antagonistic coevolution and escalation of traits that enhance females' resistance to superfluous mating and traits that increase males' persistence. How this escalation in sexually antagonistic traits is established during ontogeny remains unclear. In the water strider Rhagovelia antilleana, male persistence traits consist of sex combs on the forelegs and multiple rows of spines and a thick femur in the rear legs. Female resistance traits consist of a prominent spike-like projection of the pronotum. RNAi knockdown against the Hox gene Sex Combs Reduced resulted in the reduction in both the sex comb in males and the pronotum projection in females. RNAi against the Hox gene Ultrabithorax resulted in the complete loss or reduction of all persistence traits in male rear legs. These results demonstrate that Hox genes can be involved in intra- and inter-locus sexual conflict and mediate escalation of sexually antagonistic traits.


2020 ◽  
Author(s):  
Leonor R. Rodrigues ◽  
Mario Torralba Sáez ◽  
João Alpedrinha ◽  
Sophie Lefèvre ◽  
Muriel Brengues ◽  
...  

AbstractBoth sex allocation and sexual conflict can be modulated by spatial structure. However, how the interplay between the type of dispersal and the scale of competition simultaneously affects these traits in sub-divided populations is rarely considered.We investigated sex allocation and sexual conflict evolution in meta-populations of the spider mite Tetranychus urticae evolving under budding (pairing females from the same patch) or random (pairing females from different patches) dispersal and either local (fixed sampling from each subpopulation) versus global (sampling as a function of subpopulation productivity) competition.Females evolving under budding dispersal produced less female-biased offspring sex ratios than those from the random dispersal selection regimes, contradicting theoretical predictions. In turn, the scale of competition did not have a strong effect on sex allocation. Males evolved under budding dispersal induced less female harm than those exposed to random dispersal, but there was no reduction in female fitness following exposure to multiple mates from either selection regime.This work highlights that population structure can impact the evolution of sex allocation and sexual conflict. We also discuss how selection on either trait may reciprocally affect the evolution of the other, for example via effects on fecundity.


Author(s):  
Leonor Rodrigues ◽  
Mario Torralba Sáez ◽  
João Alpedrinha ◽  
Sophie Lefèvre ◽  
Muriel Brengues ◽  
...  

1998 ◽  
Vol 151 (1) ◽  
pp. 46-58 ◽  
Author(s):  
Paul J. Watson ◽  
Robert R. Stallmann ◽  
Göran Arnqvist

1994 ◽  
Vol 9 (8) ◽  
pp. 289-293 ◽  
Author(s):  
Locke Rowe ◽  
Göran Arnqvist ◽  
Andrew Sih ◽  
James J.Krupa

BioEssays ◽  
2014 ◽  
Vol 37 (2) ◽  
pp. 155-166 ◽  
Author(s):  
Tommaso Pizzari ◽  
Jay M. Biernaskie ◽  
Pau Carazo

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