{"title":"Recent plant photosynthate as a driver of ecological and evolutionary processes","authors":"David Johnson, Hannah M. Griffiths","doi":"10.1111/nph.71637","DOIUrl":null,"url":null,"abstract":"Summary Plants rapidly allocate carbon from photosynthesis belowground via root exudates and root‐associated microorganisms. Here we synthesise recent evidence of our understanding of the consequences of this ‘fast’ pathway of recent photosynthate flux for major ecological and evolutionary processes. This rapid input of plant‐derived carbon to soils shapes food webs and drives processes including soil CO <jats:sub>2</jats:sub> efflux, nutrient cycling, plant community dynamics, stability of symbioses and evolution of contrasting modes of nutrition, such as parasitism and mycoheterotrophy. We also highlight how seasonality and anthropogenic and natural perturbations likely determine the magnitude and dynamics of this fast pathway across major vegetation types, but these factors remain understudied. Further gaps in understanding include demonstrating causal links between photosynthate flow and key biogeochemical cycling processes and the capture of photosynthate by co‐occurring root‐associated microorganisms.","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"41 1","pages":""},"PeriodicalIF":8.7000,"publicationDate":"2026-10-18","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.71637","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Summary Plants rapidly allocate carbon from photosynthesis belowground via root exudates and root‐associated microorganisms. Here we synthesise recent evidence of our understanding of the consequences of this ‘fast’ pathway of recent photosynthate flux for major ecological and evolutionary processes. This rapid input of plant‐derived carbon to soils shapes food webs and drives processes including soil CO 2 efflux, nutrient cycling, plant community dynamics, stability of symbioses and evolution of contrasting modes of nutrition, such as parasitism and mycoheterotrophy. We also highlight how seasonality and anthropogenic and natural perturbations likely determine the magnitude and dynamics of this fast pathway across major vegetation types, but these factors remain understudied. Further gaps in understanding include demonstrating causal links between photosynthate flow and key biogeochemical cycling processes and the capture of photosynthate by co‐occurring root‐associated microorganisms.
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.