Fiona T MacNeill,Sarah G Hunter,Felicity Muth,Brian E Sedio
{"title":"花蜜代谢组有助于授粉综合征。","authors":"Fiona T MacNeill,Sarah G Hunter,Felicity Muth,Brian E Sedio","doi":"10.1111/nph.70217","DOIUrl":null,"url":null,"abstract":"'Pollination syndromes', where convergent floral signals reflect selection from a functional pollinator group, are often characterized by physical features, yet floral rewards such as nectar may also reflect selection from pollinators. We asked whether nectar chemistry shows evidence of convergence across functional pollinator groups, i.e. a 'chemical pollination syndrome'. We used untargeted metabolomics to compare nectar and leaf chemical profiles across 19 bee- and bird-syndrome species, focusing on Salvia spp. (Lamiaceae), selected to maximize switching events between pollination syndromes. We found that independently derived bird-syndrome nectar showed convergence on nectar traits distinct from bee-syndrome nectar, primarily driven by the composition and concentration of alkaloid profiles. We did not find evidence for 'passive leaking' of nectar compounds from leaves since metabolite abundances were uncorrelated across tissues and many nectar metabolites were not present in leaves. Nectar and leaf metabolomes were strongly decoupled from phylogenetic relationships within Salvia. These results suggest that functional pollinator groups may drive the evolution of floral reward chemistry, consistent with our 'chemical pollination syndrome' hypothesis and indicative of selection by pollinators, but we also consider alternative explanations. In addition, our results support the notion that nectar chemistry can be decoupled from that of other tissues.","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"32 1","pages":""},"PeriodicalIF":8.3000,"publicationDate":"2025-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Nectar metabolomes contribute to pollination syndromes.\",\"authors\":\"Fiona T MacNeill,Sarah G Hunter,Felicity Muth,Brian E Sedio\",\"doi\":\"10.1111/nph.70217\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"'Pollination syndromes', where convergent floral signals reflect selection from a functional pollinator group, are often characterized by physical features, yet floral rewards such as nectar may also reflect selection from pollinators. We asked whether nectar chemistry shows evidence of convergence across functional pollinator groups, i.e. a 'chemical pollination syndrome'. We used untargeted metabolomics to compare nectar and leaf chemical profiles across 19 bee- and bird-syndrome species, focusing on Salvia spp. (Lamiaceae), selected to maximize switching events between pollination syndromes. We found that independently derived bird-syndrome nectar showed convergence on nectar traits distinct from bee-syndrome nectar, primarily driven by the composition and concentration of alkaloid profiles. We did not find evidence for 'passive leaking' of nectar compounds from leaves since metabolite abundances were uncorrelated across tissues and many nectar metabolites were not present in leaves. Nectar and leaf metabolomes were strongly decoupled from phylogenetic relationships within Salvia. These results suggest that functional pollinator groups may drive the evolution of floral reward chemistry, consistent with our 'chemical pollination syndrome' hypothesis and indicative of selection by pollinators, but we also consider alternative explanations. In addition, our results support the notion that nectar chemistry can be decoupled from that of other tissues.\",\"PeriodicalId\":214,\"journal\":{\"name\":\"New Phytologist\",\"volume\":\"32 1\",\"pages\":\"\"},\"PeriodicalIF\":8.3000,\"publicationDate\":\"2025-05-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"New Phytologist\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1111/nph.70217\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Phytologist","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/nph.70217","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
Nectar metabolomes contribute to pollination syndromes.
'Pollination syndromes', where convergent floral signals reflect selection from a functional pollinator group, are often characterized by physical features, yet floral rewards such as nectar may also reflect selection from pollinators. We asked whether nectar chemistry shows evidence of convergence across functional pollinator groups, i.e. a 'chemical pollination syndrome'. We used untargeted metabolomics to compare nectar and leaf chemical profiles across 19 bee- and bird-syndrome species, focusing on Salvia spp. (Lamiaceae), selected to maximize switching events between pollination syndromes. We found that independently derived bird-syndrome nectar showed convergence on nectar traits distinct from bee-syndrome nectar, primarily driven by the composition and concentration of alkaloid profiles. We did not find evidence for 'passive leaking' of nectar compounds from leaves since metabolite abundances were uncorrelated across tissues and many nectar metabolites were not present in leaves. Nectar and leaf metabolomes were strongly decoupled from phylogenetic relationships within Salvia. These results suggest that functional pollinator groups may drive the evolution of floral reward chemistry, consistent with our 'chemical pollination syndrome' hypothesis and indicative of selection by pollinators, but we also consider alternative explanations. In addition, our results support the notion that nectar chemistry can be decoupled from that of other tissues.
期刊介绍:
New Phytologist is an international electronic journal published 24 times a year. It is owned by the New Phytologist Foundation, a non-profit-making charitable organization dedicated to promoting plant science. The journal publishes excellent, novel, rigorous, and timely research and scholarship in plant science and its applications. The articles cover topics in five sections: Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology. These sections encompass intracellular processes, global environmental change, and encourage cross-disciplinary approaches. The journal recognizes the use of techniques from molecular and cell biology, functional genomics, modeling, and system-based approaches in plant science. Abstracting and Indexing Information for New Phytologist includes Academic Search, AgBiotech News & Information, Agroforestry Abstracts, Biochemistry & Biophysics Citation Index, Botanical Pesticides, CAB Abstracts®, Environment Index, Global Health, and Plant Breeding Abstracts, and others.