Valérie F. Chamberland, Matías Gómez-Corrales, Kristen L. Marhaver, Pim Bongaerts, Kelly R. W. Latijnhouwers, Diana Carolina Vergara-Flórez, Skylar Snowden, Juan A. Sánchez, Mark J. A. Vermeij
Coral species abundance and biodiversity estimates are typically based on colony macromorphology. However, such measurements often underestimate the true diversity within coral communities because morphology does not necessarily reflect behavioral or genetic divergence. We previously reported on the unusual spawning behavior of the brain coral Diploria labyrinthiformis (Linnaeus, 1758) in Curaçao, Southern Caribbean, where this species spawns in both spring and autumn. Here, using data collected from 2013 to 2021, we show that in Curaçao, D. labyrinthiformis comprises two behaviorally and genetically distinct lineages, with 93% of colonies spawning exclusively in one season or the other. The two lineages could not be distinguished based on obvious macromorphological differences or depth but represented clearly distinct genetic clusters (FST = 0.098) based on genome-wide sequencing. We tested for prezygotic and postzygotic gametic barriers between them by fertilising eggs released in spring 2019 with sperm collected and cryopreserved in autumn 2018. Fertilisation in this unidirectional cross was successful and the resulting larvae developed normally, thus eliminating complete gametic incompatibility or early life postzygotic barriers as explanations for their divergence. Using observations from 19 other localities across the Wider Caribbean Region, we confirmed the co-occurrence of discrete spring- and autumn-spawning populations across a range of latitudes. Thus, we show that seasonal, temporal reproductive isolation (allochrony), but not gametic reproductive isolation, is a strong barrier to gene flow in sympatric lineages of this critically endangered reef-building coral. More broadly, our findings underscore the role of allochrony in the creation and maintenance of cryptic coral lineages and the urgency of identifying, quantifying, and conserving this diversity before it is lost.
{"title":"Discovery of Genetically Distinct, Sympatric Coral Lineages With Temporal but Not Gametic Reproductive Isolation","authors":"Valérie F. Chamberland, Matías Gómez-Corrales, Kristen L. Marhaver, Pim Bongaerts, Kelly R. W. Latijnhouwers, Diana Carolina Vergara-Flórez, Skylar Snowden, Juan A. Sánchez, Mark J. A. Vermeij","doi":"10.1111/mec.70138","DOIUrl":"10.1111/mec.70138","url":null,"abstract":"<p>Coral species abundance and biodiversity estimates are typically based on colony macromorphology. However, such measurements often underestimate the true diversity within coral communities because morphology does not necessarily reflect behavioral or genetic divergence. We previously reported on the unusual spawning behavior of the brain coral <i>Diploria labyrinthiformis</i> (Linnaeus, 1758) in Curaçao, Southern Caribbean, where this species spawns in both spring and autumn. Here, using data collected from 2013 to 2021, we show that in Curaçao, <i>D. labyrinthiformis</i> comprises two behaviorally and genetically distinct lineages, with 93% of colonies spawning exclusively in one season or the other. The two lineages could not be distinguished based on obvious macromorphological differences or depth but represented clearly distinct genetic clusters (<i>F</i><sub><i>ST</i></sub> = 0.098) based on genome-wide sequencing. We tested for prezygotic and postzygotic gametic barriers between them by fertilising eggs released in spring 2019 with sperm collected and cryopreserved in autumn 2018. Fertilisation in this unidirectional cross was successful and the resulting larvae developed normally, thus eliminating complete gametic incompatibility or early life postzygotic barriers as explanations for their divergence. Using observations from 19 other localities across the Wider Caribbean Region, we confirmed the co-occurrence of discrete spring- and autumn-spawning populations across a range of latitudes. Thus, we show that seasonal, temporal reproductive isolation (allochrony), but not gametic reproductive isolation, is a strong barrier to gene flow in sympatric lineages of this critically endangered reef-building coral. More broadly, our findings underscore the role of allochrony in the creation and maintenance of cryptic coral lineages and the urgency of identifying, quantifying, and conserving this diversity before it is lost.</p>","PeriodicalId":210,"journal":{"name":"Molecular Ecology","volume":"34 22","pages":""},"PeriodicalIF":3.9,"publicationDate":"2025-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/mec.70138","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145285205","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Maïly Kervella, Fabrice Bertile, Alexandra Granger-Farbos, Benoît Pinson, Claire Villette, Dimitri Heintz, Alain Schmitt, Martin Quque, Frédéric Bouillaud, François Criscuolo
Within the same species of eusocial insects, individuals of different castes typically display widely different life-history traits: sterile workers live for a few months, while queens can live for decades. Ageing theories emphasise the importance of metabolism and oxidative stress in explaining longevity, with mitochondrial bioenergetics standing at the crossroads of energy and reactive oxygen species production. The study of mitochondrial functioning is therefore of great relevance in determining the nature of the mechanisms that explain the contrasting longevities between insect social castes. We addressed this question in the eusocial black garden ant Lasius niger. Our findings reveal that caste differences in mitochondrial bioenergetics and the oxidative balance only partially align with oxidative stress theory predictions. Long-lived queens display lower metabolic rates and mitochondrial density, yet maintain higher cellular energy availability, as reflected by a high adenylate energy charge (AEC). This may result from enhanced mitochondrial maintenance processes and potentially a specific recourse to the purine salvage pathway, promoting ATP availability while limiting oxidative cost. Our study highlights so far unrevealed bioenergetic adaptations that might contribute to the queens' remarkable lifespan.
{"title":"Inter-Caste Comparison Reveals a Unique Bioenergetic Signature in Long-Lived Ant Queens","authors":"Maïly Kervella, Fabrice Bertile, Alexandra Granger-Farbos, Benoît Pinson, Claire Villette, Dimitri Heintz, Alain Schmitt, Martin Quque, Frédéric Bouillaud, François Criscuolo","doi":"10.1111/mec.70127","DOIUrl":"10.1111/mec.70127","url":null,"abstract":"<p>Within the same species of eusocial insects, individuals of different castes typically display widely different life-history traits: sterile workers live for a few months, while queens can live for decades. Ageing theories emphasise the importance of metabolism and oxidative stress in explaining longevity, with mitochondrial bioenergetics standing at the crossroads of energy and reactive oxygen species production. The study of mitochondrial functioning is therefore of great relevance in determining the nature of the mechanisms that explain the contrasting longevities between insect social castes. We addressed this question in the eusocial black garden ant <i>Lasius niger</i>. Our findings reveal that caste differences in mitochondrial bioenergetics and the oxidative balance only partially align with oxidative stress theory predictions. Long-lived queens display lower metabolic rates and mitochondrial density, yet maintain higher cellular energy availability, as reflected by a high adenylate energy charge (AEC). This may result from enhanced mitochondrial maintenance processes and potentially a specific recourse to the purine salvage pathway, promoting ATP availability while limiting oxidative cost. Our study highlights so far unrevealed bioenergetic adaptations that might contribute to the queens' remarkable lifespan.</p>","PeriodicalId":210,"journal":{"name":"Molecular Ecology","volume":"34 21","pages":""},"PeriodicalIF":3.9,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/mec.70127","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145273268","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Cecilia Kardum Hjort, Rachael Y. Dudaniec, Peter Olsson, Johan Ekroos, Henrik G. Smith
Anthropogenic land-use and climate change pose novel selection pressures on bees, yet their evolutionary responses in terms of morphological or physiological adaptations remain unclear. While adaptive responses are expected, these may be constrained by gene flow when changes in selection pressures are spatially heterogeneous. The buff-tailed bumblebee (Bombus terrestris) is a widespread species that copes well with anthropogenic land-use and climate change, suggesting high adaptive capacity or phenotypic plasticity. Here, we genotyped populations of native B. terrestris in south and central Sweden using RADseq to investigate genetic structure and local adaptation across a paired design of agricultural landscapes with high and low land-use complexity along a geographic climate gradient. We expected to find genetic structure reflective of regional barriers to gene flow, and molecular evidence for local adaptation to differing landscape and climate conditions. We found genetic structure separating southern Sweden from more northern regions, with a negative Tajima's D indicating a potential population expansion, likely northwards and inland into forested areas, consistent with observational data indicating a range shift. We found weak but significant evidence for local adaptation to climate and land use, specifically to agricultural land cover, including genes under putative selection linked to insecticide resistance. Signatures of selection were also identified in relation to latitude, temperature, and urban land cover, with other candidate SNPs associated with olfaction and immune response. Our results suggest that B. terrestris successfully responded to anthropogenic land-use and climate changes, likely due to its generalist traits, enabling phenotypic adaptation to changing environments.
{"title":"Landscape and Climate-Associated Selection in the Native and Widespread Bumblebee, Bombus terrestris","authors":"Cecilia Kardum Hjort, Rachael Y. Dudaniec, Peter Olsson, Johan Ekroos, Henrik G. Smith","doi":"10.1111/mec.70141","DOIUrl":"10.1111/mec.70141","url":null,"abstract":"<p>Anthropogenic land-use and climate change pose novel selection pressures on bees, yet their evolutionary responses in terms of morphological or physiological adaptations remain unclear. While adaptive responses are expected, these may be constrained by gene flow when changes in selection pressures are spatially heterogeneous. The buff-tailed bumblebee (<i>Bombus terrestris</i>) is a widespread species that copes well with anthropogenic land-use and climate change, suggesting high adaptive capacity or phenotypic plasticity. Here, we genotyped populations of native <i>B. terrestris</i> in south and central Sweden using RADseq to investigate genetic structure and local adaptation across a paired design of agricultural landscapes with high and low land-use complexity along a geographic climate gradient. We expected to find genetic structure reflective of regional barriers to gene flow, and molecular evidence for local adaptation to differing landscape and climate conditions. We found genetic structure separating southern Sweden from more northern regions, with a negative Tajima's <i>D</i> indicating a potential population expansion, likely northwards and inland into forested areas, consistent with observational data indicating a range shift. We found weak but significant evidence for local adaptation to climate and land use, specifically to agricultural land cover, including genes under putative selection linked to insecticide resistance. Signatures of selection were also identified in relation to latitude, temperature, and urban land cover, with other candidate SNPs associated with olfaction and immune response. Our results suggest that <i>B. terrestris</i> successfully responded to anthropogenic land-use and climate changes, likely due to its generalist traits, enabling phenotypic adaptation to changing environments.</p>","PeriodicalId":210,"journal":{"name":"Molecular Ecology","volume":"34 21","pages":""},"PeriodicalIF":3.9,"publicationDate":"2025-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/mec.70141","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145249109","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Matheus M. A. Salles, André L. G. Carvalho, Adam D. Leaché, Nicolas Martinez, Frederick Bauer, Martha Motte, Viviana Espínola, Miguel T. Rodrigues, Carla Piantoni, Marcio R. Pie, André Olivotto, Guarino R. Colli, Erik L. Choueri, Fernanda P. Werneck, Fabricius M. C. B. Domingos
Mitonuclear discordance—evolutionary discrepancies between mitochondrial and nuclear DNA phylogenies—can arise from various factors, including introgression, incomplete lineage sorting, recent or ancient demographic fluctuations, sex-biased dispersal asymmetries, among others. Understanding this phenomenon is crucial for accurately reconstructing evolutionary histories, as failing to account for discordance can lead to misinterpretations of species boundaries, phylogenetic relationships, and historical biogeographic patterns. We investigate the evolutionary drivers of mitonuclear discordance in the Tropidurus spinulosus species group, which contains nine species of lizards inhabiting open tropical and subtropical environments in South America. Using a combination of population genetic and phylogenomic approaches applied to mitochondrial and nuclear data, we identified different instances of gene flow that occurred in ancestral lineages of extant species. Our results point to a complex evolutionary history marked by prolonged isolation between species, demographic fluctuations, and potential episodes of secondary contact with genetic admixture. These conditions likely facilitated mitochondrial genome capture while diluting signals of nuclear introgression. Furthermore, we found no strong evidence supporting incomplete lineage sorting or natural selection as primary drivers of the observed mitonuclear discordance. Therefore, the unveiled patterns are most consistent with neutral demographic processes, coupled with ancient mitochondrial introgression, as the main factors underlying the mismatch between nuclear and mitochondrial phylogenies in this system. Future research could further explore the role of other demographic processes, such as asymmetric sex-biased dispersal, in shaping these complex evolutionary patterns.
{"title":"Ancient Introgression Explains Mitochondrial Genome Capture and Mitonuclear Discordance Among South American Collared Tropidurus Lizards","authors":"Matheus M. A. Salles, André L. G. Carvalho, Adam D. Leaché, Nicolas Martinez, Frederick Bauer, Martha Motte, Viviana Espínola, Miguel T. Rodrigues, Carla Piantoni, Marcio R. Pie, André Olivotto, Guarino R. Colli, Erik L. Choueri, Fernanda P. Werneck, Fabricius M. C. B. Domingos","doi":"10.1111/mec.70130","DOIUrl":"10.1111/mec.70130","url":null,"abstract":"<p>Mitonuclear discordance—evolutionary discrepancies between mitochondrial and nuclear DNA phylogenies—can arise from various factors, including introgression, incomplete lineage sorting, recent or ancient demographic fluctuations, sex-biased dispersal asymmetries, among others. Understanding this phenomenon is crucial for accurately reconstructing evolutionary histories, as failing to account for discordance can lead to misinterpretations of species boundaries, phylogenetic relationships, and historical biogeographic patterns. We investigate the evolutionary drivers of mitonuclear discordance in the <i>Tropidurus spinulosus</i> species group, which contains nine species of lizards inhabiting open tropical and subtropical environments in South America. Using a combination of population genetic and phylogenomic approaches applied to mitochondrial and nuclear data, we identified different instances of gene flow that occurred in ancestral lineages of extant species. Our results point to a complex evolutionary history marked by prolonged isolation between species, demographic fluctuations, and potential episodes of secondary contact with genetic admixture. These conditions likely facilitated mitochondrial genome capture while diluting signals of nuclear introgression. Furthermore, we found no strong evidence supporting incomplete lineage sorting or natural selection as primary drivers of the observed mitonuclear discordance. Therefore, the unveiled patterns are most consistent with neutral demographic processes, coupled with ancient mitochondrial introgression, as the main factors underlying the mismatch between nuclear and mitochondrial phylogenies in this system. Future research could further explore the role of other demographic processes, such as asymmetric sex-biased dispersal, in shaping these complex evolutionary patterns.</p>","PeriodicalId":210,"journal":{"name":"Molecular Ecology","volume":"34 21","pages":""},"PeriodicalIF":3.9,"publicationDate":"2025-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/mec.70130","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145249182","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}