EvolutionPub Date : 2024-12-23DOI: 10.1093/evolut/qpae187
Daniela Wilner, Jigmidmaa Boldbaatar, Soleille M Miller, Nathan W Burke, Russell Bonduriansky
{"title":"Can sexual conflict drive transitions to asexuality? Female resistance to fertilization in a facultatively parthenogenetic insect.","authors":"Daniela Wilner, Jigmidmaa Boldbaatar, Soleille M Miller, Nathan W Burke, Russell Bonduriansky","doi":"10.1093/evolut/qpae187","DOIUrl":"https://doi.org/10.1093/evolut/qpae187","url":null,"abstract":"<p><p>Facultatively parthenogenetic animals could help reveal the role of sexual conflict in the evolution of sex. Although each female can reproduce both sexually (producing sons and daughters from fertilized eggs) and asexually (typically producing only daughters from unfertilized eggs), these animals often form distinct sexual and asexual populations. We hypothesized that asexual populations are maintained through female resistance as well as the decay of male traits. We tested this via experimental crosses between individuals descended from multiple natural sexual and asexual populations of the facultatively parthenogenic stick-insect Megacrania batesii. We found that male-paired females descended from asexual populations produced strongly female-biased offspring sex-ratios resulting from reduced fertilization rates. This effect was not driven by incompatibility between diverged genotypes but, rather, by both genotypic and maternal effects on fertilization rate. Furthermore, when females from asexual populations mated and produced sons, those sons had poor fertilization success when paired with resistant females, consistent with male trait decay. Our results suggest that resistance to fertilization resulting from both maternal and genotypic effects, along with male sexual trait decay, can hinder the invasion of asexual populations by males. Sexual conflict could thus play a role in the establishment and maintenance of asexual populations.</p>","PeriodicalId":12082,"journal":{"name":"Evolution","volume":" ","pages":""},"PeriodicalIF":3.1,"publicationDate":"2024-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142876686","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
EvolutionPub Date : 2024-12-23DOI: 10.1093/evolut/qpae186
M Inam Jameel, Lisa Duncan, Kailen Mooney, Jill T Anderson
{"title":"Herbivory and water availability interact to shape the adaptive landscape in the perennial forb, Boechera stricta.","authors":"M Inam Jameel, Lisa Duncan, Kailen Mooney, Jill T Anderson","doi":"10.1093/evolut/qpae186","DOIUrl":"https://doi.org/10.1093/evolut/qpae186","url":null,"abstract":"<p><p>Abiotic and biotic factors interact to influence phenotypic evolution; however, identifying the causal agents of selection that drive the evolution and expression of traits remains challenging. In a field common garden, we manipulated water availability and herbivore abundance across three years, and evaluated clinal variation in functional traits and phenology, plasticity, local adaptation, and selection using diverse accessions of the perennial forb, Boechera stricta. Consistent with expectations, drought stress exacerbated damage from herbivores. Foliar traits exhibited greater plasticity than phenological traits, which displayed more consistent genetic clines. Water availability and herbivory interacted to exert selection, even on traits like flowering duration, which showed no clinal variation and limited plasticity. Furthermore, the direction of selection on specific leaf area in response to water availability mirrored the genetic cline and plasticity, suggesting that variation in water levels across the landscape influences the evolution of this trait. Finally, both herbivory and water availability likely contribute to local adaptation. This work emphasizes the additive and synergistic roles of abiotic and biotic factors in shaping phenotypic variation across environmental gradients.</p>","PeriodicalId":12082,"journal":{"name":"Evolution","volume":" ","pages":""},"PeriodicalIF":3.1,"publicationDate":"2024-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142876689","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
EvolutionPub Date : 2024-12-23DOI: 10.1093/evolut/qpae185
Yanqian Ding, Chris Metherell, Wu Huang, Peter M Hollingsworth, Alex D Twyford
{"title":"Genome-wide differentiation by geography not species in taxonomically complex eyebrights (Euphrasia).","authors":"Yanqian Ding, Chris Metherell, Wu Huang, Peter M Hollingsworth, Alex D Twyford","doi":"10.1093/evolut/qpae185","DOIUrl":"https://doi.org/10.1093/evolut/qpae185","url":null,"abstract":"<p><p>Most studies investigating the genomic nature of species differences anticipate monophyletic species with genome-wide differentiation. However, this may not be the case at the earliest stages of speciation where reproductive isolation is weak and homogenising gene flow blurs species boundaries. We investigate genomic differences between species in a postglacial radiation of eyebrights (Euphrasia), a taxonomically complex plant group with variation in ploidy and mating system. We use genotyping-by-sequencing and spatially-aware clustering methods to investigate genetic structure across 378 populations from 18 British and Irish Euphrasia species. We find only northern Scottish populations of the selfing heathland specialist E. micrantha demonstrate genome-wide divergence from other species. Instead of genetic clusters corresponding to species, all other clusters align with geographic regions, such as a genetic cluster on Shetland that includes ten tetraploid species. Recent divergence and extensive gene flow between putative species is supported by a lack of species-specific SNPs or clear outlier loci. We anticipate a similar lack of association between genomic clusters and species identities may occur in other recent postglacial groups. Where new species emerge this is associated with a transition in mating system or novel ecological preferences.</p>","PeriodicalId":12082,"journal":{"name":"Evolution","volume":" ","pages":""},"PeriodicalIF":3.1,"publicationDate":"2024-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142876688","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
EvolutionPub Date : 2024-12-22DOI: 10.1093/evolut/qpae158
Antoine M Dujon, Amy M Boddy, Rodrigo Hamede, Beata Ujvari, Frédéric Thomas
{"title":"Beyond Peto's paradox: expanding the study of cancer resistance across species.","authors":"Antoine M Dujon, Amy M Boddy, Rodrigo Hamede, Beata Ujvari, Frédéric Thomas","doi":"10.1093/evolut/qpae158","DOIUrl":"10.1093/evolut/qpae158","url":null,"abstract":"<p><p>Peto's paradox, which highlights the lower-than-expected cancer rates in larger and/or longer-lived species, is a cornerstone of discussions at the intersection of ecology, evolution, and cancer research. It prompts investigations into how species with traits that theoretically increase cancer risk manage to exhibit cancer resistance, with the ultimate goal of uncovering novel therapies for humans. Building on these foundational insights, we propose expanding the research focus to species that, despite possessing traits beyond size and longevity that theoretically increase their cancer risk, exhibit unexpected cancer resistance. Testing Peto's paradox without interference from transient dynamics also requires considering species that are at an equilibrium between cancer risks and defenses, which is increasingly challenging due to anthropogenic activities. Additionally, we argue that transmissible cancers could significantly help in understanding how the metastatic process might be naturally suppressed. This research perspective is timely and aims to support the continued and in-depth identification of anti-cancer adaptations retained throughout evolution in the animal kingdom.</p>","PeriodicalId":12082,"journal":{"name":"Evolution","volume":" ","pages":"6-10"},"PeriodicalIF":3.1,"publicationDate":"2024-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142568243","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
EvolutionPub Date : 2024-12-22DOI: 10.1093/evolut/qpae150
Frank Johannes
{"title":"Allometric scaling of somatic mutation and epimutation rates in trees.","authors":"Frank Johannes","doi":"10.1093/evolut/qpae150","DOIUrl":"10.1093/evolut/qpae150","url":null,"abstract":"<p><p>How long-lived trees escape \"mutational meltdown\" despite centuries of continuous growth remains puzzling. Here we integrate recent studies to show that the yearly rate of somatic mutations and epimutations (μY) scales inversely with generation time (G), and follows the same allometric power law found in mammals (μY ∝ G-1). Deeper insights into the scaling function may permit predictions of somatic (epi)mutation rates from life-history traits without the need for genomic data.</p>","PeriodicalId":12082,"journal":{"name":"Evolution","volume":" ","pages":"1-5"},"PeriodicalIF":3.1,"publicationDate":"2024-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142461276","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
EvolutionPub Date : 2024-12-22DOI: 10.1093/evolut/qpae142
Alexandre Casadei-Ferreira, Gabriela Procópio Camacho, Thomas van de Kamp, John E Lattke, Rodrigo Machado Feitosa, Evan P Economo
{"title":"Evolution and functional implications of stinger shape in ants.","authors":"Alexandre Casadei-Ferreira, Gabriela Procópio Camacho, Thomas van de Kamp, John E Lattke, Rodrigo Machado Feitosa, Evan P Economo","doi":"10.1093/evolut/qpae142","DOIUrl":"10.1093/evolut/qpae142","url":null,"abstract":"<p><p>Trait diversification is often driven by underlying performance tradeoffs in the context of different selective pressures. Evolutionary changes in task specialization may influence how species respond to tradeoffs and alter diversification. We conducted this study to investigate the functional morphology, evolutionary history, and tempo and mode of evolution of the Hymenoptera stinger using Ectatomminae ants as a model clade. We hypothesized that a performance tradeoff surface underlies the diversity of stinger morphology and that shifts between predatory and omnivorous diets mediate the diversification dynamics of the trait. Shape variation was characterized by X-ray microtomography, and the correlation between shape and average values of von Mises stress, as a measure of yield failure criteria under loading conditions typical of puncture scenarios, was determined using finite element analysis. We observed that stinger elongation underlies most of the shape variation but found no evidence of biomechanical tradeoffs in the performance characteristics measured. In addition, omnivores have increased phenotypic shifts and accelerated evolution in performance metrics, suggesting the evolution of dietary flexibility releases selection pressure on a specific function, resulting in a greater phenotypic evolutionary rate. These results increase our understanding of the biomechanical basis of stinger shape, indicate that shape diversity is not the outcome of simple biomechanical optimization, and reveal connections between diet and trait diversification.</p>","PeriodicalId":12082,"journal":{"name":"Evolution","volume":" ","pages":"80-99"},"PeriodicalIF":3.1,"publicationDate":"2024-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142375348","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
EvolutionPub Date : 2024-12-22DOI: 10.1093/evolut/qpae146
Emily E K Kopania, Gregg W C Thomas, Carl R Hutter, Sebastian M E Mortimer, Colin M Callahan, Emily Roycroft, Anang S Achmadi, William G Breed, Nathan L Clark, Jacob A Esselstyn, Kevin C Rowe, Jeffrey M Good
{"title":"Sperm competition intensity shapes divergence in both sperm morphology and reproductive genes across murine rodents.","authors":"Emily E K Kopania, Gregg W C Thomas, Carl R Hutter, Sebastian M E Mortimer, Colin M Callahan, Emily Roycroft, Anang S Achmadi, William G Breed, Nathan L Clark, Jacob A Esselstyn, Kevin C Rowe, Jeffrey M Good","doi":"10.1093/evolut/qpae146","DOIUrl":"10.1093/evolut/qpae146","url":null,"abstract":"<p><p>It remains unclear how variation in the intensity of sperm competition shapes phenotypic and molecular evolution across clades. Mice and rats in the subfamily Murinae are a rapid radiation exhibiting incredible diversity in sperm morphology and production. We combined phenotypic and genomic data to perform phylogenetic comparisons of male reproductive traits and genes across 78 murine species. We identified several shifts towards smaller relative testes mass (RTM), presumably reflecting reduced sperm competition. Several sperm traits were associated with RTM, suggesting that mating system evolution selects for convergent suites of traits related to sperm competitive ability. We predicted that sperm competition would also drive more rapid molecular divergence in species with large testes. Contrary to this, we found that many spermatogenesis genes evolved more rapidly in species with smaller RTM due to relaxed purifying selection. While some reproductive genes evolved rapidly under recurrent positive selection, relaxed selection played a greater role in underlying rapid evolution in small testes species. Our work demonstrates that postcopulatory sexual selection can impose strong purifying selection shaping the evolution of male reproduction and that broad patterns of molecular evolution may help identify genes that contribute to male fertility.</p>","PeriodicalId":12082,"journal":{"name":"Evolution","volume":" ","pages":"11-27"},"PeriodicalIF":3.1,"publicationDate":"2024-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142406287","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
EvolutionPub Date : 2024-12-22DOI: 10.1093/evolut/qpae138
Antoine Laboury, Thomas L Stubbs, Andrzej S Wolniewicz, Jun Liu, Torsten M Scheyer, Marc E H Jones, Valentin Fischer
{"title":"Contrasting macroevolutionary patterns in pelagic tetrapods across the Triassic-Jurassic transition.","authors":"Antoine Laboury, Thomas L Stubbs, Andrzej S Wolniewicz, Jun Liu, Torsten M Scheyer, Marc E H Jones, Valentin Fischer","doi":"10.1093/evolut/qpae138","DOIUrl":"10.1093/evolut/qpae138","url":null,"abstract":"<p><p>The iconic marine raptorial predators Ichthyosauria and Eosauropterygia co-existed in the same ecosystems throughout most of the Mesozoic Era, facing similar evolutionary pressures and environmental perturbations. Both groups seemingly went through a massive macroevolutionary bottleneck across the Triassic-Jurassic (T/J) transition that greatly reduced their morphological diversity, leaving pelagic lineages as the only survivors. However, analyses of marine reptile disparity across the T/J transition have usually employed coarse morphological and temporal data. We comprehensively compare the evolution of ichthyosaurian and eosauropterygian morphology and body size across the Middle Triassic to Early Jurassic interval and find contrasting macroevolutionary patterns. The ecomorphospace of eosauropterygians predominantly reflects a strong phylogenetic signal, resulting in the clustering of three clades with clearly distinct craniodental phenotypes, suggesting \"leaps\" toward novel feeding ecologies. Ichthyosaurian diversification lacks a discernible evolutionary trend, as we find evidence for a wide overlap of craniodental morphologies between Triassic and Early Jurassic forms. The temporal evolution of ecomorphological disparity, fin shape and body size of eosauropterygians and ichthyosaurians during the Late Triassic does not support the hypothesis of an abrupt macroevolutionary bottleneck near the T/J transition. Rather, an important turnover event should be sought earlier, during times of rapid sea level falls.</p>","PeriodicalId":12082,"journal":{"name":"Evolution","volume":" ","pages":"38-50"},"PeriodicalIF":3.1,"publicationDate":"2024-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142282504","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
EvolutionPub Date : 2024-12-22DOI: 10.1093/evolut/qpae137
Zhongyi Yao, Kun Huang, Yin Qi, Jinzhong Fu
{"title":"Does brain size of Asiatic toads (Bufo gargarizans) trade-off with other energetically expensive organs along altitudinal gradients?","authors":"Zhongyi Yao, Kun Huang, Yin Qi, Jinzhong Fu","doi":"10.1093/evolut/qpae137","DOIUrl":"10.1093/evolut/qpae137","url":null,"abstract":"<p><p>Brain size variation is often attributed to energetic trade-offs with other metabolically expensive tissues and organs, which is a prediction of the expensive brain hypothesis (EBH). Here we examine Asiatic toads (Bufo gargarizans) along altitudinal gradients and test size trade-offs between the brain and four visceral organs (heart, liver, alimentary tract, and kidney) with altitude. Body size and scaled mass index (a proxy for total energy intake) decline with altitude, implying stronger energetic constraints at high altitudes. Relative brain size decreases along altitudinal gradients, while visceral organs mostly increase in relative sizes. Using structural equation modeling, a significant negative relationship between brain size and a latent variable \"budget,\" which represents the energy allocation to the four visceral organs, is detected among high-altitudinal toads. Heart appears to have the largest and most consistent response to changes in energy allocation. No such relationships are observed among toads at middle- and low-altitudes, where high energy intake may allow individuals to forego energetic trade-offs. When applying EBH to poikilotherms, a great emphasis should be placed on total energy intake in addition to energy allocation. Future research on EBH will benefit from more intra-specific comparisons and the evaluation of fitness consequences beyond energy limitation.</p>","PeriodicalId":12082,"journal":{"name":"Evolution","volume":" ","pages":"28-37"},"PeriodicalIF":3.1,"publicationDate":"2024-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142282505","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
EvolutionPub Date : 2024-12-22DOI: 10.1093/evolut/qpae154
Jan T Lifjeld, Emily R A Cramer, Erica H Leder, Kjetil Lysne Voje
{"title":"Sperm as a speciation phenotype in promiscuous songbirds.","authors":"Jan T Lifjeld, Emily R A Cramer, Erica H Leder, Kjetil Lysne Voje","doi":"10.1093/evolut/qpae154","DOIUrl":"10.1093/evolut/qpae154","url":null,"abstract":"<p><p>Sperm morphology varies considerably among species. Sperm traits may contribute to speciation if they diverge fast in allopatry and cause conspecific sperm precedence upon secondary contact. However, their role in driving prezygotic isolation has been poorly investigated. Here we test the hypothesis that, early in the speciation process, female promiscuity promotes a reduction in overlap in sperm length distributions among songbird populations. We assembled a data set of 20 pairs of populations with known sperm length distributions, a published estimate of divergence time, and an index of female promiscuity derived from extrapair paternity rates or relative testis size. We found that sperm length distributions diverged more rapidly in more promiscuous species. Faster divergence between sperm length distributions was caused by the lower variance in the trait in more promiscuous species, and not by faster divergence of the mean sperm lengths. The reduced variance is presumably due to stronger stabilizing selection on sperm length mediated by sperm competition. If divergent sperm length optima in allopatry causes conspecific sperm precedence in sympatry, which remains to be shown empirically, female promiscuity may promote prezygotic isolation, and rapid speciation in songbirds.</p>","PeriodicalId":12082,"journal":{"name":"Evolution","volume":" ","pages":"134-143"},"PeriodicalIF":3.1,"publicationDate":"2024-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142557429","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}