scholarly journals Conspecific sperm precedence is reinforced but sexual selection weakened in sympatric populations ofDrosophila

2016 ◽  
Author(s):  
Dean M. Castillo ◽  
Leonie C. Moyle

SUMMARYSexual selection is well recognized as a driver of reproductive isolation between lineages. However, selection for increased reproductive isolation could reciprocally change the outcomes of sexual selection, when these processes share a genetic basis. Direct selection for reproductive isolation occurs in the context of ‘reinforcement’, where selection acts to increase prezygotic barriers to reduce the cost of heterospecific matings. Many studies of reinforcement focus on premating reproductive barriers, however postmating traits-such as conspecific sperm precedence (CSP)-can also respond to reinforcing selection. We tested whether i) CSP responded to reinforcing selection, and ii) this response in sympatric populations altered intraspecific sperm competition (ISC) and the strength of sexual selection, with the sister speciesDrosophila pseudoobscuraandD. persimilis. We used sperm competition experiments to evaluate differences in CSP and ISC between two sympatric and two allopatric populations ofD. pseudoobscura. Using multiple genotypes for each population allowed us to estimate not only patterns of phenotype divergence, but also the opportunity for sexual selection within each population. Consistent with a pattern of reinforcement, the sympatric populations had higher mean CSP. Moreover, ISC was altered in sympatric populations, where we observed decreased average offensive sperm competitive ability against conspecific males, allowing less opportunity for sexual selection to operate within these populations. These data demonstrate that strong reinforcing selection for reproductive isolation can have consequences for sexual selection and sexual interactions within species, in these important postmating sperm competition traits.

2019 ◽  
Vol 286 (1899) ◽  
pp. 20182535 ◽  
Author(s):  
Dean M. Castillo ◽  
Leonie C. Moyle

Sexual selection can accelerate speciation by driving the evolution of reproductive isolation, but forces driving speciation could also reciprocally feedback on sexual selection. This might be particularly important in the context of ‘reinforcement’, where selection acts directly to increase prezygotic barriers to reduce the cost of heterospecific matings. Using assays of sperm competition within and between two sister species, we show a signature of reinforcement where these species interact: populations of Drosophila pseudoobscura that co-occur with sister species D. persimilis have an elevated ability to outcompete heterospecific sperm, consistent with selection for increased postcopulatory isolation. We also find these D. pseudoobscura populations have decreased sperm competitive ability against conspecifics, reducing the opportunity for sexual selection within these populations. Our findings demonstrate that direct selection to increase reproductive isolation against other species can compromise the efficacy of sexual selection within species, a collateral effect of reproductive traits responding to heterospecific interactions.


2014 ◽  
Vol 281 (1797) ◽  
pp. 20142050 ◽  
Author(s):  
Dean M. Castillo ◽  
Leonie C. Moyle

Sexual selection and sexual conflict are considered important drivers of speciation, based on both theoretical models and empirical correlations between sexually selected traits and diversification. However, whether reproductive isolation between species evolves directly as a consequence of intrapopulation sexual dynamics remains empirically unresolved, in part because knowledge of the genetic mechanisms (if any) connecting these processes is limited. Here, we provide evidence of a direct mechanistic link between intraspecies sexual selection and reproductive isolation. We examined genes with known roles in intraspecific sperm competition (ISC) in D. melanogaster and assayed their impact on conspecific sperm precedence (CSP). We found that two such genes ( Acp36DE and CG9997 ) contribute to both offensive sperm competition and CSP; null/knockdown lines both had lower competitive ability against D. melanogaster conspecifics and were no longer able to displace heterospecific D. simulans sperm in competitive matings. In comparison, Sex Peptide ( Acp70A )—another locus essential for ISC—does not contribute to CSP. These data indicate that two loci important for sperm competitive interactions have an additional role in similar interactions that enforce post-mating reproductive isolation between species, and show that sexual selection and sexual isolation can act on the same molecular targets in a gene-specific manner.


2011 ◽  
Vol 279 (1729) ◽  
pp. 826-832 ◽  
Author(s):  
John J. Lees ◽  
Robert L. Nudds ◽  
Lars P. Folkow ◽  
Karl-Arne Stokkan ◽  
Jonathan R. Codd

Little is known regarding the physiological consequences of the behavioural and morphological differences that result from sexual selection in birds. Male and female Svalbard rock ptarmigans ( Lagopus muta hyperborea ) exhibit distinctive behavioural differences during the breeding season. In particular, males continuously compete for and defend territories in order to breed successfully, placing large demands on their locomotor system. Here, we demonstrate that male birds have improved locomotor performance compared with females, showing both a lower cost of locomotion (CoL) and a higher top speed. We propose that the observed sex differences in locomotor capability may be due to sexual selection for improved male performance. While the mechanisms underlying these energetic differences are unclear, future studies should be wary when pooling male and female data.


2013 ◽  
Vol 280 (1755) ◽  
pp. 20122863 ◽  
Author(s):  
Jeff Clune ◽  
Jean-Baptiste Mouret ◽  
Hod Lipson

A central biological question is how natural organisms are so evolvable (capable of quickly adapting to new environments). A key driver of evolvability is the widespread modularity of biological networks—their organization as functional, sparsely connected subunits—but there is no consensus regarding why modularity itself evolved. Although most hypotheses assume indirect selection for evolvability, here we demonstrate that the ubiquitous, direct selection pressure to reduce the cost of connections between network nodes causes the emergence of modular networks. Computational evolution experiments with selection pressures to maximize network performance and minimize connection costs yield networks that are significantly more modular and more evolvable than control experiments that only select for performance. These results will catalyse research in numerous disciplines, such as neuroscience and genetics, and enhance our ability to harness evolution for engineering purposes.


Behaviour ◽  
1990 ◽  
Vol 115 (1-2) ◽  
pp. 100-113 ◽  
Author(s):  
W. Andy Snedden

AbstractThe large chelipeds of male Orconectes rusticus have an adaptive function related to inter-male competition for mates. Large clawed males dominate over smaller clawed, but otherwise physically similar, competitors. Additionally, males with large chela are better able to secure, and more quickly orient, females into the copulatory position. Large clawed males also copulate for longer periods than smaller clawed competitors. The significance of copulation duration is unclear, but is likely related to mate guarding. Sexual selection for increased cheliped size in 0. rusticus has been more intense on males than females. Sperm of the second male to inseminate a dually mated female takes precedence over that of the previous male. The paternity attributable to the second male was determined as approximately 92 % .


2021 ◽  
Author(s):  
Avani Mital ◽  
Manaswini Sarangi ◽  
Bodhisatta Nandy ◽  
Neha Pandey ◽  
Amitabh Joshi

The role of sexual selection in mediating levels of sexual conflict has been demonstrated in a number of experimental evolution studies on Drosophila sp. where the level of competition among males for fertilization success was under direct selection. Here we report that selection for a short development time and early age at reproduction can lead to inadvertent changes in levels of sexual selection in D. melanogaster populations, affecting reproductive competition experienced by males. We demonstrate that faster developing and early reproducing populations showed very low levels of mating in their lifetime (likely being monogamous), low courtship levels, shorter copulation duration and longer maturation time, compared to their ancestral controls. We discuss these results in light of the previously demonstrated reduction of sexual conflict in these populations.


2007 ◽  
Vol 274 (1612) ◽  
pp. 983-988 ◽  
Author(s):  
Paul F Rugman-Jones ◽  
Paul E Eady

Conspecific sperm precedence (CSP) has been identified as an important post-copulatory, pre-zygotic mechanism that can act to reduce gene flow between populations. The evolution of CSP is thought to have arisen as a by-product of male and female coevolution in response to intraspecific post-copulatory sexual selection. However, little is known about the mechanisms that generate CSP. When Callosobruchus subinnotatus females copulate with both C. subinnotatus and Callosobruchus maculatus males, regardless of mating order, the majority of eggs are fertilized by conspecific sperm. The low number of heterospecific fertilizations does not result from general differences in the viability of sperm in the female reproductive tract, as heterospecific sperm fertilized equivalent numbers of eggs as conspecific sperm in the absence of sperm competition. Instead, CSP results from disadvantages to heterospecific sperm that are manifest only when in competition with conspecific sperm. CSP in C. subinnotatus appears to result from two, not mutually exclusive, mechanisms. First, conspecific sperm are better able to displace heterospecific sperm from female storage. Second, conspecific sperm achieve disproportionately higher numbers of fertilizations relative to their proportional representation in the fertilization set. Thus, we provide evidence of differential sperm use from the female spermatheca.


2002 ◽  
Vol 79 (1) ◽  
pp. 65-74 ◽  
Author(s):  
ALBERTO CIVETTA ◽  
HEIDI M. WALDRIP-DAIL ◽  
ANDREW G. CLARK

The progeny of Drosophila females doubly-mated to males from the same and a closely related species are mostly sired by conspecific males. We examined the genetic basis for conspecific mating preference and sperm precedence by using 186 Drosophila lines in which random chromosomal fragments of D. sechellia were introgressed into D. simulans. Sperm competition was measured for each of these lines by crossing ebony D. simulans female with ebony D. simulans males followed by wild-type males from the introgressed lines. Variation in sperm competition (proportion of progeny sired by the second male), mating discrimination (proportion of introgressed males that failed to remate), and male fecundity (proportion of progeny sired by introgressed males) were scored. The introgressed lines exhibited highly significant heterogeneity in the three phenotypes scored, motivating an analysis to locate quantitative trait loci (QTLs) responsible for the differences. Applying composite interval mapping, we found eight QTLs that explain a significant level of variation among introgressed lines in the phenotypes scored. Cytological position overlapped among some QTLs suggesting possible pleiotropic effects. Analysis of the joint effects of simulans/sechellia genetic composition at different QTLs and markers suggests that complex interactions among alleles are partially responsible for interspecific differences in sexual traits.


2020 ◽  
Vol 375 (1813) ◽  
pp. 20200071 ◽  
Author(s):  
Martin D. Garlovsky ◽  
Leeban H. Yusuf ◽  
Michael G. Ritchie ◽  
Rhonda R. Snook

Postcopulatory sexual selection can generate evolutionary arms races between the sexes resulting in the rapid coevolution of reproductive phenotypes. As traits affecting fertilization success diverge between populations, postmating prezygotic (PMPZ) barriers to gene flow may evolve. Conspecific sperm precedence is a form of PMPZ isolation thought to evolve early during speciation yet has mostly been studied between species. Here , we show conpopulation sperm precedence (CpSP) between Drosophila montana populations. Using Pool-seq genomic data we estimate divergence times and ask whether PMPZ isolation evolved in the face of gene flow. We find models incorporating gene flow fit the data best indicating populations experienced considerable gene flow during divergence. We find CpSP is asymmetric and mirrors asymmetry in non-competitive PMPZ isolation, suggesting these phenomena have a shared mechanism. However, we show asymmetry is unrelated to the strength of postcopulatory sexual selection acting within populations. We tested whether overlapping foreign and coevolved ejaculates within the female reproductive tract altered fertilization success but found no effect. Our results show that neither time since divergence nor sperm competitiveness predicts the strength of PMPZ isolation. We suggest that instead cryptic female choice or mutation-order divergence may drive divergence of postcopulatory phenotypes resulting in PMPZ isolation. This article is part of the theme issue ‘Fifty years of sperm competition’.


Ecoscience ◽  
1996 ◽  
Vol 3 (3) ◽  
pp. 280-284 ◽  
Author(s):  
Karine Picard ◽  
Marco Festa-Bianchet ◽  
Donald Thomas

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