scholarly journals SIGNAL TRAIT SEXUAL DIMORPHISM AND MUTUAL SEXUAL SELECTION IN DROSOPHILA SERRATA

Evolution ◽  
2003 ◽  
Vol 57 (10) ◽  
pp. 2326-2334 ◽  
Author(s):  
Stephen F. Chenoweth ◽  
Mark W. Blows
Evolution ◽  
2003 ◽  
Vol 57 (10) ◽  
pp. 2326 ◽  
Author(s):  
Stephen F. Chenoweth ◽  
Mark W. Blows

Evolution ◽  
1983 ◽  
Vol 37 (1) ◽  
pp. 96 ◽  
Author(s):  
Jerry F. Downhower ◽  
Luther Brown ◽  
Ronald Pederson ◽  
Gloria Staples

2021 ◽  
Author(s):  
Stephen P. De Lisle

AbstractA well-known property of sexual selection combined with a cross sex genetic correlation (rmf), is that it can facilitate a peak shift on the adaptive landscape. How do these diversifying effects of sexual selection +rmf balance with the constraints imposed by such sexual antagonism, to affect macroevolution of sexual dimorphism? Here, I extend existing quantitative genetic models of evolution on complex adaptive landscapes. Beyond recovering classical predictions for the conditions promoting a peak shift, I show that when rmf is moderate to strong, relatively weak sexual selection is required to induce a peak shift in males only. Increasing the strength of sexual leads to a sexually-concordant peak shift, suggesting that macroevolutionary rates of sexual dimorphism may be largely decoupled from the strength of within-population sexual selection. Accounting explicitly for demography further reveals that sex-specific peak shifts may be more likely to be successful than concordant shifts in the face of extinction, especially when natural selection is strong. An overarching conclusion is that macroevolutionary patterns of sexual dimorphism are unlikely to be readily explained by within-population estimates of selection or constraint alone.


2021 ◽  
Vol 288 (1960) ◽  
Author(s):  
Adam J. Reddiex ◽  
Stephen F. Chenoweth

In evolutionary quantitative genetics, the genetic variance–covariance matrix, G , and the vector of directional selection gradients, β , are key parameters for predicting multivariate selection responses and genetic constraints. Historically, investigations of G and β have not overlapped with those dissecting the genetic basis of quantitative traits. Thus, it remains unknown whether these parameters reflect pleiotropic effects at individual loci. Here, we integrate multivariate genome-wide association study (GWAS) with G and β estimation in a well-studied system of multivariate constraint: sexual selection on male cuticular hydrocarbons (CHCs) in Drosophila serrata . In a panel of wild-derived re-sequenced lines, we augment genome-based restricted maximum likelihood to estimate G alongside multivariate single nucleotide polymorphism (SNP) effects, detecting 532 significant associations from 1 652 276 SNPs. Constraint was evident, with β lying in a direction of G with low evolvability. Interestingly, minor frequency alleles typically increased male CHC-attractiveness suggesting opposing natural selection on β . SNP effects were significantly misaligned with the major eigenvector of G , g max , but well aligned to the second and third eigenvectors g 2 and g 3 . We discuss potential factors leading to these varied results including multivariate stabilizing selection and mutational bias. Our framework may be useful as researchers increasingly access genomic methods to study multivariate selection responses in wild populations.


2006 ◽  
Vol 75 (03-04) ◽  
pp. 189-194 ◽  
Author(s):  
Ronald Vonk ◽  
Vincent Nijman

Small populations of several species of the groundwater dwelling amphipod genus Ingolfiella are found in caves, wells, seabottoms, beaches and riverbed interstitial habitats. To gain insight in the socio-ecology of these elusive species, we used data from collected specimens to explore the relationships between sexratios, display of secondary sexual characters and other morphological features, and habitat use. We extracted data on the sex ratios and the presence-absence of secondary sexual characters of 13 species from the literature and through examination of museum material. We found a clearly skewed sex ratio with a preponderance of females, both in the individual species as in the genus as a whole. However, sex ratio and the display of secondary sexual characters were not correlated, nor did these characters correlate with the amount of sexual dimorphism. It remains unknown why so many ingolfiellids have evolved these costly features.


2012 ◽  
Vol 2 (2) ◽  
pp. 287-297 ◽  
Author(s):  
Ann J. Stocker ◽  
Bosco B. Rusuwa ◽  
Mark J. Blacket ◽  
Francesca D. Frentiu ◽  
Mitchell Sullivan ◽  
...  

2007 ◽  
Vol 274 (1617) ◽  
pp. 1553-1560 ◽  
Author(s):  
O Krüger ◽  
N.B Davies ◽  
M.D Sorenson

Sexual dimorphism is ubiquitous in animals and can result from selection pressure on one or both sexes. Sexual selection has become the predominant explanation for the evolution of sexual dimorphism, with strong selection on size-related mating success in males being the most common situation. The cuckoos (family Cuculidae) provide an exceptional case in which both sexes of many species are freed from the burden of parental care but where coevolution between parasitic cuckoos and their hosts also results in intense selection. Here, we show that size and plumage differences between the sexes in parasitic cuckoos are more likely the result of coevolution than sexual selection. While both sexes changed in size as brood parasitism evolved, we find no evidence for selection on males to become larger. Rather, our analysis indicates stronger selection on parasitic females to become smaller, resulting in a shift from dimorphism with larger females in cuckoos with parental care to dimorphism with larger males in parasitic species. In addition, the evolution of brood parasitism was associated with more cryptic plumage in both sexes, but especially in females, a result that contrasts with the strong plumage dimorphism seen in some other parasitic birds. Examination of the three independent origins of brood parasitism suggests that different parasitic cuckoo lineages followed divergent evolutionary pathways to successful brood parasitism. These results argue for the powerful role of parasite–host coevolution in shaping cuckoo life histories in general and sexual dimorphism in particular.


Author(s):  
P. Vermeiren ◽  
C. Lennard ◽  
C. Trave

Abstract Intertidal crabs display distinct morphological traits that allow differential interactions with biotic and abiotic features of the intertidal landscape, but are also influenced by allometry and sexual selection. This study aimed to explore the influence of sexual, allometric and habitat factors on morphological variation in the intertidal mangrove crab assemblage. A standardized photographic protocol was developed using readily available, low-cost technology to capture the morphology of carapaces and claws as sets of Cartesian landmarks. Digitization errors were 1 to 2 orders of magnitude smaller than the variation among individuals. In Tubuca seismella and Tubuca signata (superfamily Ocypodoidea), species that have traditionally been studied for sexual dimorphism, standardized major claw sizes were 2.8 and 3.7, respectively, times larger for males than females. Sexual dimorphism in claw size was also observed for Metopograpsus frontalis and Parasesarma longicristatum (superfamily Grapsoidea), with the largest claw in males being 15% and 33%, respectively, larger than in females. In contrast to size, claw shape did not relate to sex, except for T. seismella. Carapace shape, although variable among individuals and displaying asymmetry, was unrelated to sex. Claw and carapace shapes displayed high correlations, with values around 0.78. Carapace shapes grouped into taxonomic families and linked to habitat preferences, while claw shapes varied along a taxonomic gradient. These results complement studies on crab morphology that focus on specific factors or species, and stress the importance of multiple, interacting factors including sexual, allometric and habitat influences as drivers of morphological trait variability.


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