Mating tactics and male wing dimorphism in the damselfly,Mnais pruinosa costalis selys (Odonata: Calopterygidae)

1990 ◽  
Vol 8 (2) ◽  
pp. 129-137 ◽  
Author(s):  
Mamoru Watanabe ◽  
Masao Taguchi
2017 ◽  
Author(s):  
Binshuang Li ◽  
Ryan D. Bickel ◽  
Benjamin J. Parker ◽  
Neetha Nanoth Vellichirammal ◽  
Mary Grantham ◽  
...  

SummaryWing dimorphisms have long served as models for examining the ecological and evolutionary tradeoffs associated with alternative morphologies [1], yet the mechanistic basis of morph determination remains largely unknown. Here we investigate the genetic basis of the pea aphid (Acyrthosiphon pisum) wing dimorphism, wherein males exhibit one of two alternative morphologies that differ dramatically in a set of correlated traits that inclused the presence or absence of wings [2-4]. Unlike the environmentally-induced asexual female aphid wing polyphenism [5], the male wing polymorphism is genetically determined by a single uncharacterized locus on the X chromosome called aphicarus (“aphid” plus “Icarus”, api) [6, 7]. Using recombination and association mapping, we localized api to a 130kb region of the pea aphid genome. No nonsynonymous variation in coding sequences strongly associated with the winged and wingless phenotypes, indicating that api is likely a regulatory change. Gene expression level profiling revealed an aphid-specific gene from the region expressed at higher levels in winged male embryos, coinciding with the expected stage of api action. Comparison of the api region across biotypes (pea aphid populations specialized to different host plants that began diverging ~16,000 years ago [8, 9]) revealed that the two alleles were likely present prior to biotype diversification. Moreover, we find evidence for a recent selective sweep of a wingless allele since the biotypes diversified. In sum, this study provides insight into how adaptive, complex traits evolve within and across natural populations.


eLife ◽  
2020 ◽  
Vol 9 ◽  
Author(s):  
Binshuang Li ◽  
Ryan D Bickel ◽  
Benjamin J Parker ◽  
Omid Saleh Ziabari ◽  
Fangzhou Liu ◽  
...  

Wing dimorphisms have long served as models for examining the ecological and evolutionary tradeoffs associated with alternative phenotypes. Here, we investigated the genetic cause of the pea aphid (Acyrthosiphon pisum) male wing dimorphism, wherein males exhibit one of two morphologies that differ in correlated traits that include the presence or absence of wings. We mapped this trait difference to a single genomic region and, using third generation, long-read sequencing, we identified a 120 kb insertion in the wingless allele. This insertion includes a duplicated follistatin gene, which is a strong candidate gene in the minimal mapped interval to cause the dimorphism. We found that both alleles were present prior to pea aphid biotype lineage diversification, we estimated that the insertion occurred millions of years ago, and we propose that both alleles have been maintained in the species, likely due to balancing selection.


2019 ◽  
Author(s):  
Binshuang Li ◽  
Ryan D Bickel ◽  
Benjamin J Parker ◽  
Omid Saleh Ziabari ◽  
Fangzhou Liu ◽  
...  

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

2021 ◽  
Vol 18 (1) ◽  
Author(s):  
Lenka Sentenská ◽  
Aileen Neumann ◽  
Yael Lubin ◽  
Gabriele Uhl

Abstract Background Mating generally occurs after individuals reach adulthood. In many arthropods including spiders, the adult stage is marked by a final moult after which the genitalia are fully developed and functional. In several widow spider species (genus Latrodectus), however, immature females may mate a few days before they moult to adulthood, i.e. in their late-subadult stage. While the “adult” mating typically results in cannibalism, males survive the “immature” mating. During both “immature” and “adult” matings, males leave parts of their paired copulatory organs within female genitalia, which may act as mating plugs. To study potential costs and benefits of the two mating tactics, we investigated female genital morphology of the brown widow spider, L. geometricus. Light microscopy, histology and micro-computed tomography of early-subadult, late-subadult and adult females were conducted to determine the overall pattern of genital maturation. We compared genitalia of mated late-subadult and adult females to reveal potential differences in the genitalic details that might indicate differential success in sperm transfer and different environments for sperm storage and sperm competition. Results We found that the paired sperm storage organs (spermathecae) and copulatory ducts are developed already in late-subadult females and host sperm after immature mating. However, the thickness of the spermathecal cuticle and the staining of the secretions inside differ significantly between the late-subadult and adult females. In late-subadult females mating plugs were found with higher probability in both spermathecae compared to adult females. Conclusions Sperm transfer in matings with late-subadult females follows the same route as in matings with adult females. The observed differences in the secretions inside the spermathecae of adult and late-subadult females likely reflect different storage conditions for the transferred sperm which may lead to a disadvantage under sperm competition if the subadult female later re-mates with another male. However, since males mating with late-subadult females typically transfer sperm to both spermathecae they might benefit from numerical sperm competition as well as from monopolizing access to the female sperm storage organs. The assessment of re-mating probability and relative paternity will clarify the costs and benefits of the two mating tactics in light of these findings.


2005 ◽  
Vol 83 (12) ◽  
pp. 1638-1642 ◽  
Author(s):  
Albrecht I Schulte-Hostedde ◽  
Gary Burness

Sperm competition results in the evolution of ejaculate characteristics such as high sperm density, high motility, and fast sperm swimming speed. A fundamental assumption of sperm competition theory is that ejaculates with high motility and fast-swimming sperm have an advantage with respect to fertilization success. We tested this assumption by studying the fertilization dynamics of alternative mating tactics (cuckolders and parentals) of male bluegill (Lepomis macrochirus Rafinesque, 1819). Sneakers (cuckolders) have faster swimming sperm and a higher proportion of motile sperm immediately following sperm activation than do parentals; however, these variables decline more quickly over time in sneaker sperm than in the sperm of parental males. We used a controlled fertilization experiment to test the prediction that parental males will have higher fertilization success than sneakers late in the sperm activation cycle because of the reduced rate of decline in ejaculate quality over time. We found that as the time from sperm activation increases parental sperm fertilizes more eggs than the sperm of sneakers. Our results support the idea that fertilization success is higher when ejaculates contain a higher proportion of either motile sperm or faster swimming sperm, all else being equal. In addition, after controlling for time from sperm activation, we found a significant bias in fertilization success toward parental males, suggesting that cryptic female choice might play a role in fertilization dynamics.


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