Pub Date : 2026-03-24DOI: 10.1038/s41559-026-03020-6
Peter I. Macreadie, George E. Biddulph, Pere Masque, Hilary Kennedy, Jimena Samper-Villarreal, J. Patrick Megonigal, Hannah K. Morrissette, Tania E. Romero-Gonzalez, Vanessa Hatje, Jana Friedrich, Sigit D. Sasmito, Kenta Watanabe, Inés Mazarrasa, Dorte Krause-Jensen, Janine B. Adams, Miguel Cifuentes-Jara, Ariane Arias-Ortiz, Andre S. Rovai, Milica Stankovic, Kirsten Isensee, Ana M. Queirós, Luzhen Chen, Jorge Herrera-Silveira, Catriona L. Hurd, Rashid Ismail, Ken W. Krauss, Anna Lafratta, Maria M. Palacios, William E. N. Austin
Blue carbon ecosystems, classically defined as mangroves, tidal marshes and seagrasses, but increasingly expanded to include ecosystems such as tidal flats, macroalgal forests and shelf sediments, contribute to climate change mitigation and biodiversity support. Here, seven years after the last global assessment of research priorities, we conducted a priority-setting exercise to identify persistent knowledge and implementation gaps, and the strategic priorities that must be addressed to enable scalable, high-integrity and equitable management of blue carbon ecosystems in a rapidly evolving policy and finance landscape. The highest priority focuses on managing blue carbon ecosystems to support coastal communities while integrating traditional ecological knowledge, emphasizing the essential role of social legitimacy and equity in enabling scalable, long-lasting outcomes. Additional priorities focus on developing cost-effective restoration methods, improving the accuracy of greenhouse gas flux estimates, quantifying the impacts of human activities on carbon cycling and integrating co-benefits such as biodiversity and coastal protection into natural capital frameworks. Emerging technologies like remote sensing, machine learning and data-sharing platforms are also highlighted as transformative tools to fill knowledge gaps and scale solutions. Collectively, these priorities highlight the complexity of blue carbon science and the need for inclusive interdisciplinary approaches that support the resilience and livelihoods of coastal communities.
{"title":"Priority questions for the next decade of blue carbon science","authors":"Peter I. Macreadie, George E. Biddulph, Pere Masque, Hilary Kennedy, Jimena Samper-Villarreal, J. Patrick Megonigal, Hannah K. Morrissette, Tania E. Romero-Gonzalez, Vanessa Hatje, Jana Friedrich, Sigit D. Sasmito, Kenta Watanabe, Inés Mazarrasa, Dorte Krause-Jensen, Janine B. Adams, Miguel Cifuentes-Jara, Ariane Arias-Ortiz, Andre S. Rovai, Milica Stankovic, Kirsten Isensee, Ana M. Queirós, Luzhen Chen, Jorge Herrera-Silveira, Catriona L. Hurd, Rashid Ismail, Ken W. Krauss, Anna Lafratta, Maria M. Palacios, William E. N. Austin","doi":"10.1038/s41559-026-03020-6","DOIUrl":"https://doi.org/10.1038/s41559-026-03020-6","url":null,"abstract":"Blue carbon ecosystems, classically defined as mangroves, tidal marshes and seagrasses, but increasingly expanded to include ecosystems such as tidal flats, macroalgal forests and shelf sediments, contribute to climate change mitigation and biodiversity support. Here, seven years after the last global assessment of research priorities, we conducted a priority-setting exercise to identify persistent knowledge and implementation gaps, and the strategic priorities that must be addressed to enable scalable, high-integrity and equitable management of blue carbon ecosystems in a rapidly evolving policy and finance landscape. The highest priority focuses on managing blue carbon ecosystems to support coastal communities while integrating traditional ecological knowledge, emphasizing the essential role of social legitimacy and equity in enabling scalable, long-lasting outcomes. Additional priorities focus on developing cost-effective restoration methods, improving the accuracy of greenhouse gas flux estimates, quantifying the impacts of human activities on carbon cycling and integrating co-benefits such as biodiversity and coastal protection into natural capital frameworks. Emerging technologies like remote sensing, machine learning and data-sharing platforms are also highlighted as transformative tools to fill knowledge gaps and scale solutions. Collectively, these priorities highlight the complexity of blue carbon science and the need for inclusive interdisciplinary approaches that support the resilience and livelihoods of coastal communities.","PeriodicalId":18835,"journal":{"name":"Nature ecology & evolution","volume":"275 1","pages":""},"PeriodicalIF":16.8,"publicationDate":"2026-03-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147506146","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-24DOI: 10.1038/s41559-026-03029-x
James Gahan, Helen F. Yan, David R. Bellwood, Graham J. Edgar, Leo Nankervis, Alexandre C. Siqueira, Rick D. Stuart-Smith, Sterling B. Tebbett
The functioning of high-diversity ecosystems, such as coral reefs, is intrinsically tied to the integrity and efficiency of the trophic pathways within these systems. Coral reef productivity depends, in part, on the input of external nutrients, primarily zooplankton, that is assimilated by extraordinarily diverse fish communities. The plankton–planktivore trophic pathway is thus crucial for sustaining the productivity that exemplifies coral reef ecosystems; however, it remains poorly understood at large spatial scales. Here we explore global patterns in reef fish community structure, revealing a major discrepancy between the Indo-Pacific and Caribbean in the productivity and fisheries potential of planktivorous reef fishes. Indo-Pacific reefs support 6.6 times more planktivorous fish biomass and 3.4 times greater productivity than the Caribbean, a difference largely due to the marked contribution of species that feed on gelatinous plankton in the Indo-Pacific. Although species that feed on gelatinous plankton constitute only 4% of the planktivorous fish abundance in the Indo-Pacific, they account for one-third of the biomass and one-quarter of the productivity. This divergence reflects the contrasting biogeographic histories of the two realms, with Indo-Pacific oceanography fostering diversification, while repeated extinction events and trophic erosion may have constrained planktivory in the Caribbean. Ultimately, these differences in energy flow translate into fundamental differences in coral reef functioning and, potentially, their capacity to support ecosystem services, including fisheries.
{"title":"Missing planktivore functions drive global variation in reef fish productivity","authors":"James Gahan, Helen F. Yan, David R. Bellwood, Graham J. Edgar, Leo Nankervis, Alexandre C. Siqueira, Rick D. Stuart-Smith, Sterling B. Tebbett","doi":"10.1038/s41559-026-03029-x","DOIUrl":"https://doi.org/10.1038/s41559-026-03029-x","url":null,"abstract":"The functioning of high-diversity ecosystems, such as coral reefs, is intrinsically tied to the integrity and efficiency of the trophic pathways within these systems. Coral reef productivity depends, in part, on the input of external nutrients, primarily zooplankton, that is assimilated by extraordinarily diverse fish communities. The plankton–planktivore trophic pathway is thus crucial for sustaining the productivity that exemplifies coral reef ecosystems; however, it remains poorly understood at large spatial scales. Here we explore global patterns in reef fish community structure, revealing a major discrepancy between the Indo-Pacific and Caribbean in the productivity and fisheries potential of planktivorous reef fishes. Indo-Pacific reefs support 6.6 times more planktivorous fish biomass and 3.4 times greater productivity than the Caribbean, a difference largely due to the marked contribution of species that feed on gelatinous plankton in the Indo-Pacific. Although species that feed on gelatinous plankton constitute only 4% of the planktivorous fish abundance in the Indo-Pacific, they account for one-third of the biomass and one-quarter of the productivity. This divergence reflects the contrasting biogeographic histories of the two realms, with Indo-Pacific oceanography fostering diversification, while repeated extinction events and trophic erosion may have constrained planktivory in the Caribbean. Ultimately, these differences in energy flow translate into fundamental differences in coral reef functioning and, potentially, their capacity to support ecosystem services, including fisheries.","PeriodicalId":18835,"journal":{"name":"Nature ecology & evolution","volume":"27 1","pages":""},"PeriodicalIF":16.8,"publicationDate":"2026-03-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147506145","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-20DOI: 10.1038/s41559-026-03037-x
Xiaoyu Yang,Guanjing Cai,Runlin Cai,Haifeng Gu,Yuerong Chen,Jianmin Xie,Zhong Hu,Jonathan Y S Leung,Hanno Teeling,Hui Wang
Dinoflagellates and diatoms are key marine phytoplankton, with ecological roles strongly influenced by their associated phycosphere bacteria. However, the ecophysiological functions of these bacteria remain enigmatic as a result of insufficient taxonomic and genomic characterization. Here, by combining single-cell isolation with a custom statistical pipeline, we profiled resident bacterial communities associated with 108 diatom and 86 dinoflagellate strains, collected across temperate and tropical oceans worldwide. We examined genomic traits of key bacterial populations through whole-genome sequencing of representative isolates. Taxonomic compositions of dinoflagellate- and diatom-associated microbiota were distinct, highlighting host-specific differences. Each microbiota harboured characteristic genera with adaptive traits reflecting host metabolic profiles. Dinoflagellate-associated bacteria were enriched in genes responsible for motility and sulfur-compound use, whereas diatom-associated bacteria specialized in glycan use. We identified 'foundation' genera, defined as taxa with high occupancy and community-level impact in both phycosphere types (for example, Marivita and Marinobacter), sharing host-specific traits with characteristic bacteria while universally excelling in environmental response and resistance. Notably, foundation bacteria were enriched in Type VI secretion systems, emerging as a universal hallmark of phycosphere bacteria across global oceans. Overall, this study provides insights into the taxonomic and metabolic nature of phycosphere bacteria, highlighting the profound influences of interspecific interactions on marine ecological processes.
{"title":"Taxonomic composition and ecophysiology of resident bacteria associated with marine phytoplankton.","authors":"Xiaoyu Yang,Guanjing Cai,Runlin Cai,Haifeng Gu,Yuerong Chen,Jianmin Xie,Zhong Hu,Jonathan Y S Leung,Hanno Teeling,Hui Wang","doi":"10.1038/s41559-026-03037-x","DOIUrl":"https://doi.org/10.1038/s41559-026-03037-x","url":null,"abstract":"Dinoflagellates and diatoms are key marine phytoplankton, with ecological roles strongly influenced by their associated phycosphere bacteria. However, the ecophysiological functions of these bacteria remain enigmatic as a result of insufficient taxonomic and genomic characterization. Here, by combining single-cell isolation with a custom statistical pipeline, we profiled resident bacterial communities associated with 108 diatom and 86 dinoflagellate strains, collected across temperate and tropical oceans worldwide. We examined genomic traits of key bacterial populations through whole-genome sequencing of representative isolates. Taxonomic compositions of dinoflagellate- and diatom-associated microbiota were distinct, highlighting host-specific differences. Each microbiota harboured characteristic genera with adaptive traits reflecting host metabolic profiles. Dinoflagellate-associated bacteria were enriched in genes responsible for motility and sulfur-compound use, whereas diatom-associated bacteria specialized in glycan use. We identified 'foundation' genera, defined as taxa with high occupancy and community-level impact in both phycosphere types (for example, Marivita and Marinobacter), sharing host-specific traits with characteristic bacteria while universally excelling in environmental response and resistance. Notably, foundation bacteria were enriched in Type VI secretion systems, emerging as a universal hallmark of phycosphere bacteria across global oceans. Overall, this study provides insights into the taxonomic and metabolic nature of phycosphere bacteria, highlighting the profound influences of interspecific interactions on marine ecological processes.","PeriodicalId":18835,"journal":{"name":"Nature ecology & evolution","volume":"13 1","pages":""},"PeriodicalIF":16.8,"publicationDate":"2026-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147490148","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-18DOI: 10.1038/s41559-026-03046-w
Kate T Snyder, Aleyna Loughran-Pierce, Nicole Creanza
{"title":"Publisher Correction: Territoriality modulates the coevolution of cooperative breeding and female song in songbirds.","authors":"Kate T Snyder, Aleyna Loughran-Pierce, Nicole Creanza","doi":"10.1038/s41559-026-03046-w","DOIUrl":"https://doi.org/10.1038/s41559-026-03046-w","url":null,"abstract":"","PeriodicalId":18835,"journal":{"name":"Nature ecology & evolution","volume":" ","pages":""},"PeriodicalIF":13.9,"publicationDate":"2026-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147481185","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-16DOI: 10.1038/s41559-026-03014-4
Zheng Zhou (周正), Nico Eisenhauer, Andrew D. Barnes, Melanie M. Pollierer, Malte Jochum, Ingo Grass, Yan Zhang, Ulrich Brose, Fujio Hyodo, Nicole Scheunemann, Olaf Schmidt, Yuanyuan Huang, Bernhard Klarner, Anton A. Goncharov, Alena Krause, Daniil Korobushkin, Anastasia Gorbunova, Ilya I. Lyubechanskii, Sergey M. Tsurikov, Julia Seeber, Michael Steinwandter, Vladimir A. Zryanin, Oksana L. Rozanova, Winda Ika Susanti, Felicity V. Crotty, Di Ajeng Prameswari, Zhipeng Li, Carol Melody, Zhijing Xie, Xue Pan, Donghui Wu, Mark Maraun, Katerina Sam, Alexei V. Tiunov, Stefan Scheu, Anton Potapov
Soil fauna contributes to a wide range of ecosystem functions via their trophic activities. Here we investigate how trophic diversity of soil animals varies across functional groups and major biomes. We use stable isotope analysis (13C/12C and 15N/14N ratios) of 17,306 samples of 28 high-rank taxa from 456 sites across 19 countries to inspect the variability in trophic diversity across climate regions and land-use types. Trophic diversity of soil animal communities is higher for microbial feeders than for detritivores and predators, in agricultural ecosystems compared with woodlands (+32%) and in tropical compared with temperate climates (+40%). Higher trophic diversity is related to more diverse basal resources and longer trophic chains, which could reflect greater niche partitioning in resource-limited environments. Our findings suggest that soil animals could broaden their trophic niches under agricultural land use and possibly in response to warming, but whether such foraging flexibility may offset the loss of trophic specialists remains to be investigated.
{"title":"Greater trophic diversity of soil animal communities under agricultural land use and tropical climate","authors":"Zheng Zhou \u0000 (周正), Nico Eisenhauer, Andrew D. Barnes, Melanie M. Pollierer, Malte Jochum, Ingo Grass, Yan Zhang, Ulrich Brose, Fujio Hyodo, Nicole Scheunemann, Olaf Schmidt, Yuanyuan Huang, Bernhard Klarner, Anton A. Goncharov, Alena Krause, Daniil Korobushkin, Anastasia Gorbunova, Ilya I. Lyubechanskii, Sergey M. Tsurikov, Julia Seeber, Michael Steinwandter, Vladimir A. Zryanin, Oksana L. Rozanova, Winda Ika Susanti, Felicity V. Crotty, Di Ajeng Prameswari, Zhipeng Li, Carol Melody, Zhijing Xie, Xue Pan, Donghui Wu, Mark Maraun, Katerina Sam, Alexei V. Tiunov, Stefan Scheu, Anton Potapov","doi":"10.1038/s41559-026-03014-4","DOIUrl":"https://doi.org/10.1038/s41559-026-03014-4","url":null,"abstract":"Soil fauna contributes to a wide range of ecosystem functions via their trophic activities. Here we investigate how trophic diversity of soil animals varies across functional groups and major biomes. We use stable isotope analysis (13C/12C and 15N/14N ratios) of 17,306 samples of 28 high-rank taxa from 456 sites across 19 countries to inspect the variability in trophic diversity across climate regions and land-use types. Trophic diversity of soil animal communities is higher for microbial feeders than for detritivores and predators, in agricultural ecosystems compared with woodlands (+32%) and in tropical compared with temperate climates (+40%). Higher trophic diversity is related to more diverse basal resources and longer trophic chains, which could reflect greater niche partitioning in resource-limited environments. Our findings suggest that soil animals could broaden their trophic niches under agricultural land use and possibly in response to warming, but whether such foraging flexibility may offset the loss of trophic specialists remains to be investigated.","PeriodicalId":18835,"journal":{"name":"Nature ecology & evolution","volume":"11 1","pages":""},"PeriodicalIF":16.8,"publicationDate":"2026-03-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147465723","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-13DOI: 10.1038/s41559-026-03017-1
Arnaud N’Guessan, Vivian Wang, Christopher W. Bakerlee, Jenya Belousova, Greta Y.-S. Brenna, Megan E. Dillingham, Shreyas Gopalakrishnan, Juhee Goyal, Misha Gupta, Caroline M. Holmes, Parris T. Humphrey, Tanush Jagdish, Elizabeth R. Jerison, Milo S. Johnson, Katya Kosheleva, Katherine R. Lawrence, Jiseon Min, Alief Moulana, Shreyas V. Pai, Angela M. Phillips, Julia C. Piper, Ramya Purkanti, Artur Rego-Costa, Tatiana Ruiz-Bedoya, Cecilia Trivellin, Michael J. McDonald, Michael M. Desai, Alex N. Nguyen Ba
Experimental evolution has been a useful tool for investigating long-term temporal evolutionary dynamics and molecular mechanisms underlying adaptation. However, extracting fundamental principles and predictive features of evolutionary outcomes from these datasets remains challenging. Here we sought to circumvent these challenges by comparing distant yeast species that share several evolutionary features but differ in evolutionary history and genome architecture, that is Saccharomyces cerevisiae and Schizosaccharomyces pombe. We evolved ten populations of the fission yeast for 10,000 generations in the same conditions as a pre-existing budding yeast dataset, allowing us to observe repeatable evolutionary outcomes within species but diverse molecular targets of adaptation across species. The most frequent route of adaptation was through changes in carbon flux metabolism, which was previously unseen in S. cerevisiae evolved populations, but similar evolutionary paths have been observed in wild populations. This suggests that parallelism is pervasive and that mechanisms of adaptation can be shared among closely related or distant species. Despite similar gene content and identical environments, recurrent adaptation across S. pombe populations involved different genes than in S. cerevisiae and was detectable mostly at the transcriptomic level. This indicates that trans-regulatory effects and contingency may contribute to differences in evolutionary outcomes between these species.
{"title":"Parallel but distinct adaptive routes in the budding and fission yeasts after 10,000 generations of experimental evolution","authors":"Arnaud N’Guessan, Vivian Wang, Christopher W. Bakerlee, Jenya Belousova, Greta Y.-S. Brenna, Megan E. Dillingham, Shreyas Gopalakrishnan, Juhee Goyal, Misha Gupta, Caroline M. Holmes, Parris T. Humphrey, Tanush Jagdish, Elizabeth R. Jerison, Milo S. Johnson, Katya Kosheleva, Katherine R. Lawrence, Jiseon Min, Alief Moulana, Shreyas V. Pai, Angela M. Phillips, Julia C. Piper, Ramya Purkanti, Artur Rego-Costa, Tatiana Ruiz-Bedoya, Cecilia Trivellin, Michael J. McDonald, Michael M. Desai, Alex N. Nguyen Ba","doi":"10.1038/s41559-026-03017-1","DOIUrl":"https://doi.org/10.1038/s41559-026-03017-1","url":null,"abstract":"Experimental evolution has been a useful tool for investigating long-term temporal evolutionary dynamics and molecular mechanisms underlying adaptation. However, extracting fundamental principles and predictive features of evolutionary outcomes from these datasets remains challenging. Here we sought to circumvent these challenges by comparing distant yeast species that share several evolutionary features but differ in evolutionary history and genome architecture, that is Saccharomyces cerevisiae and Schizosaccharomyces pombe. We evolved ten populations of the fission yeast for 10,000 generations in the same conditions as a pre-existing budding yeast dataset, allowing us to observe repeatable evolutionary outcomes within species but diverse molecular targets of adaptation across species. The most frequent route of adaptation was through changes in carbon flux metabolism, which was previously unseen in S. cerevisiae evolved populations, but similar evolutionary paths have been observed in wild populations. This suggests that parallelism is pervasive and that mechanisms of adaptation can be shared among closely related or distant species. Despite similar gene content and identical environments, recurrent adaptation across S. pombe populations involved different genes than in S. cerevisiae and was detectable mostly at the transcriptomic level. This indicates that trans-regulatory effects and contingency may contribute to differences in evolutionary outcomes between these species.","PeriodicalId":18835,"journal":{"name":"Nature ecology & evolution","volume":"10 1","pages":""},"PeriodicalIF":16.8,"publicationDate":"2026-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147454762","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-11DOI: 10.1038/s41559-026-03004-6
Alex Cagan
As somatic evolution becomes directly measurable, integrating eco-evolutionary principles with high-resolution molecular data creates opportunities to anticipate and prevent disease.
随着躯体进化变得可以直接测量，将生态进化原理与高分辨率分子数据相结合，为预测和预防疾病创造了机会。
{"title":"How somatic evolution affects health","authors":"Alex Cagan","doi":"10.1038/s41559-026-03004-6","DOIUrl":"10.1038/s41559-026-03004-6","url":null,"abstract":"As somatic evolution becomes directly measurable, integrating eco-evolutionary principles with high-resolution molecular data creates opportunities to anticipate and prevent disease.","PeriodicalId":18835,"journal":{"name":"Nature ecology & evolution","volume":"10 3","pages":"392-394"},"PeriodicalIF":13.9,"publicationDate":"2026-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.comhttps://www.nature.com/articles/s41559-026-03004-6.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147388724","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}
Pub Date : 2026-03-11DOI: 10.1038/s41559-025-02953-8
Filipe Abreu
Witnessing the effects of yellow fever virus in Brazil motivates Filipe Abreu’s work.
目睹黄热病病毒在巴西的影响促使Filipe Abreu开展工作。
{"title":"Yellow fever virus","authors":"Filipe Abreu","doi":"10.1038/s41559-025-02953-8","DOIUrl":"10.1038/s41559-025-02953-8","url":null,"abstract":"Witnessing the effects of yellow fever virus in Brazil motivates Filipe Abreu’s work.","PeriodicalId":18835,"journal":{"name":"Nature ecology & evolution","volume":"10 3","pages":"609-609"},"PeriodicalIF":13.9,"publicationDate":"2026-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147388718","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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