Yang Liu, Charity Mangoi, Zhichao Dong, Hui Ma, Wei Li, Lars L Iversen, Yu Cao
{"title":"Heterophyllous plants reorganize plant trait coordination between floating and emergent habitats.","authors":"Yang Liu, Charity Mangoi, Zhichao Dong, Hui Ma, Wei Li, Lars L Iversen, Yu Cao","doi":"10.1016/j.plaphy.2026.111364","DOIUrl":null,"url":null,"abstract":"<p><p>Plant structures function as integrated modules, reflecting coordinated development and function across traits. In terrestrial plants, stomatal traits that regulate carbon uptake are tightly coordinated with xylem traits supplying water, maintaining trade-offs between photosynthetic demand and hydraulic capacity. In aquatic plants, however, contrasting environments experienced by emergent and floating leaves may alter these coordination patterns. Whether heterophylly modifies fundamental scaling relationships among traits remains unclear. Here, we examined 15 heterophyllous aquatic species that produce both floating and emergent leaves within the same individual, allowing isolated effects from phylogeny. We found that emergent leaves exhibited greater leaf area, total stomatal area, and petiole thickness, indicating increased hydraulic and mechanical investment. Both leaf types followed hypoallometric scaling between leaf and petiole traits, but coordination regimes diverged. Emergent leaves showed tighter scaling between total stomatal area and petiole xylem area, reflecting strengthened coupling between transpirational demand and hydraulic supply. In contrast, floating leaves exhibited steeper scaling between leaf area and petiole transverse area and a more centralized trait network structure. These divergences persisted after accounting for phylogeny. Together, our results showed that heterophyllous plants could maintain core developmental proportionality while reorganizing trait coordination in response to different habitats.</p>","PeriodicalId":20234,"journal":{"name":"Plant Physiology and Biochemistry","volume":"234 ","pages":"111364"},"PeriodicalIF":5.7000,"publicationDate":"2026-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Physiology and Biochemistry","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.plaphy.2026.111364","RegionNum":2,"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
Plant structures function as integrated modules, reflecting coordinated development and function across traits. In terrestrial plants, stomatal traits that regulate carbon uptake are tightly coordinated with xylem traits supplying water, maintaining trade-offs between photosynthetic demand and hydraulic capacity. In aquatic plants, however, contrasting environments experienced by emergent and floating leaves may alter these coordination patterns. Whether heterophylly modifies fundamental scaling relationships among traits remains unclear. Here, we examined 15 heterophyllous aquatic species that produce both floating and emergent leaves within the same individual, allowing isolated effects from phylogeny. We found that emergent leaves exhibited greater leaf area, total stomatal area, and petiole thickness, indicating increased hydraulic and mechanical investment. Both leaf types followed hypoallometric scaling between leaf and petiole traits, but coordination regimes diverged. Emergent leaves showed tighter scaling between total stomatal area and petiole xylem area, reflecting strengthened coupling between transpirational demand and hydraulic supply. In contrast, floating leaves exhibited steeper scaling between leaf area and petiole transverse area and a more centralized trait network structure. These divergences persisted after accounting for phylogeny. Together, our results showed that heterophyllous plants could maintain core developmental proportionality while reorganizing trait coordination in response to different habitats.
期刊介绍:
Plant Physiology and Biochemistry publishes original theoretical, experimental and technical contributions in the various fields of plant physiology (biochemistry, physiology, structure, genetics, plant-microbe interactions, etc.) at diverse levels of integration (molecular, subcellular, cellular, organ, whole plant, environmental). Opinions expressed in the journal are the sole responsibility of the authors and publication does not imply the editors'' agreement.
Manuscripts describing molecular-genetic and/or gene expression data that are not integrated with biochemical analysis and/or actual measurements of plant physiological processes are not suitable for PPB. Also "Omics" studies (transcriptomics, proteomics, metabolomics, etc.) reporting descriptive analysis without an element of functional validation assays, will not be considered. Similarly, applied agronomic or phytochemical studies that generate no new, fundamental insights in plant physiological and/or biochemical processes are not suitable for publication in PPB.
Plant Physiology and Biochemistry publishes several types of articles: Reviews, Papers and Short Papers. Articles for Reviews are either invited by the editor or proposed by the authors for the editor''s prior agreement. Reviews should not exceed 40 typewritten pages and Short Papers no more than approximately 8 typewritten pages. The fundamental character of Plant Physiology and Biochemistry remains that of a journal for original results.