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/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/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":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11663510/pdf/","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":"OA","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}
EvolutionPub Date : 2024-12-22DOI: 10.1093/evolut/qpae156
Karin Gross
{"title":"Digest: Scarce pollen resources and asymmetric reproductive isolation.","authors":"Karin Gross","doi":"10.1093/evolut/qpae156","DOIUrl":"10.1093/evolut/qpae156","url":null,"abstract":"<p><p>What mechanisms cause asymmetries in reproductive success in crosses between closely related species that differ in floral style length? Feller et al. (2024) found that in 5 Phlox species, short-styled species produced smaller pollen grains than long-styled species. The smaller pollen of short-styled species lacked the resources to grow pollen tubes long enough to reach the ovules of long-styled species. This asymmetric pollen-style-length incompatibility may considerably affect patterns of gene flow among species.</p>","PeriodicalId":12082,"journal":{"name":"Evolution","volume":" ","pages":"153-154"},"PeriodicalIF":3.1,"publicationDate":"2024-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142564170","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/qpae139
Maria R Servedio
{"title":"The contributions of direct and indirect selection to the evolution of mating preferences.","authors":"Maria R Servedio","doi":"10.1093/evolut/qpae139","DOIUrl":"10.1093/evolut/qpae139","url":null,"abstract":"<p><p>Many influential mathematical models of sexual selection have stressed that mating preferences evolve due to correlations that build between mating preferences and preferred display traits-that is, through indirect selection. Nevertheless, there is a perception that indirect selection should generally be overwhelmed by direct selection, for example, in the form of search costs. Recent work by Fry has used quantitative genetic models to argue that in many cases, including when there are direct benefits (a fecundity advantage to mating with the preferred male), direct and indirect selection may be of similar magnitude. Here, I use population genetic models, in which the strength of the genetic correlation is an emergent property of evolution at mating preference and display trait loci, to assess the relative contributions of direct and indirect selection to the evolution of mating preferences. For the cases of direct benefits and of indirect benefits with fixed and frequency-dependent search costs, I outline parameter values of fecundity benefits, preference strengths, and search costs for which indirect selection on female preferences can potentially predominate. I also analyze male mate choice under polygyny, showing that direct selection will always outweigh indirect selection except when there are direct benefits.</p>","PeriodicalId":12082,"journal":{"name":"Evolution","volume":" ","pages":"51-64"},"PeriodicalIF":3.1,"publicationDate":"2024-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142344232","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/qpae143
Dale T Clement, Dylan G Gallinson, Rodrigo K Hamede, Menna E Jones, Mark J Margres, Hamish McCallum, Andrew Storfer
{"title":"Coevolution promotes the coexistence of Tasmanian devils and a fatal, transmissible cancer.","authors":"Dale T Clement, Dylan G Gallinson, Rodrigo K Hamede, Menna E Jones, Mark J Margres, Hamish McCallum, Andrew Storfer","doi":"10.1093/evolut/qpae143","DOIUrl":"10.1093/evolut/qpae143","url":null,"abstract":"<p><p>Emerging infectious diseases threaten natural populations, and data-driven modeling is critical for predicting population dynamics. Despite the importance of integrating ecology and evolution in models of host-pathogen dynamics, there are few wild populations for which long-term ecological datasets have been coupled with genome-scale data. Tasmanian devil (Sarcophilus harrisii) populations have declined range wide due to devil facial tumor disease (DFTD), a fatal transmissible cancer. Although early ecological models predicted imminent devil extinction, diseased devil populations persist at low densities, and recent ecological models predict long-term devil persistence. Substantial evidence supports the evolution of both devils and DFTD, suggesting coevolution may also influence continued devil persistence. Thus, we developed an individual-based, eco-evolutionary model of devil-DFTD coevolution parameterized with nearly 2 decades of devil demography, DFTD epidemiology, and genome-wide association studies. We characterized potential devil-DFTD coevolutionary outcomes and predicted the effects of coevolution on devil persistence and devil-DFTD coexistence. We found a high probability of devil persistence over 50 devil generations (100 years) and a higher likelihood of devil-DFTD coexistence, with greater devil recovery than predicted by previous ecological models. These novel results add to growing evidence for long-term devil persistence and highlight the importance of eco-evolutionary modeling for emerging infectious diseases.</p>","PeriodicalId":12082,"journal":{"name":"Evolution","volume":" ","pages":"100-118"},"PeriodicalIF":3.1,"publicationDate":"2024-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142389157","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/qpae144
Nandita Chaturvedi, Purba Chatterjee
{"title":"Evolutionary Adaptation in Heterogeneous and Changing Environments.","authors":"Nandita Chaturvedi, Purba Chatterjee","doi":"10.1093/evolut/qpae144","DOIUrl":"10.1093/evolut/qpae144","url":null,"abstract":"<p><p>Organisms that are adapting to long-term environmental change almost always deal with multiple environments and trade-offs that affect their optimal phenotypic strategy. Here, we combine the idea of repeated variation or heterogeneity, like seasonal shifts, with long-term directional dynamics. Using the framework of fitness sets, we determine the dynamics of the optimal phenotype in two competing environments encountered with different frequencies, one of which changes with time. When such an optimal strategy is selected for in simulations of evolving populations, we observe rich behavior that is qualitatively different from and more complex than adaptation to long-term change in a single environment. The probability of survival and the critical rate of environmental change above which populations go extinct depend crucially on the relative frequency of the two environments and the strength and asymmetry of their selection pressures. We identify a critical frequency for the stationary environment, above which populations can escape the pressure to constantly evolve by adapting to the stationary optimum. In the neighborhood of this critical frequency, we also find the counter-intuitive possibility of a lower bound on the rate of environmental change, below which populations go extinct, and above which a process of evolutionary rescue is possible.</p>","PeriodicalId":12082,"journal":{"name":"Evolution","volume":" ","pages":"119-133"},"PeriodicalIF":3.1,"publicationDate":"2024-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142389158","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}