Aleca M Borsuk, Josh M Randall, Jennifer Richburg, Kyra G Montes, Erika J Edwards, Craig R Brodersen
{"title":"Palisade cell geometry in relation to leaf optical and photosynthetic properties in Viburnum.","authors":"Aleca M Borsuk, Josh M Randall, Jennifer Richburg, Kyra G Montes, Erika J Edwards, Craig R Brodersen","doi":"10.1093/plphys/kiae659","DOIUrl":null,"url":null,"abstract":"<p><p>The optical properties of lobed palisade mesophyll cells remain poorly understood despite their presence in diverse taxa and the critical role of the palisade layer in leaf-light interactions and carbon assimilation. Using micro-computed tomography, 3D ray tracing simulations, and physiological experiments, we tested the interactions between palisade cell geometry, chloroplast localization, light directional quality, and leaf optical and photosynthetic performance in the model taxon Viburnum. Simulations showed that lobed cells shifted between absorptance- or transmittance-dominated states depending on chloroplast localization, irrespective of light directional quality. In contrast, columnar palisade optics were driven by light directional quality, with absorptance-dominated properties under diffuse light and transmittance-dominated properties under direct light, irrespective of chloroplast localization. Lobed palisade cells in planta were less densely packed yet more productive on a per cell basis than columnar palisade cells, resulting in interspecific conservation of maximum carbon assimilation rate per unit leaf tissue. For the Viburnum species studied, our results indicate a 'many-to-one' mapping of multiple palisade cell forms to a common rate of photosynthetic productivity per unit tissue. This work highlights the dynamic relationship between palisade mesophyll form and function and informs the anatomical basis of plant carbon assimilation.</p>","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":" ","pages":""},"PeriodicalIF":6.5000,"publicationDate":"2024-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/plphys/kiae659","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
The optical properties of lobed palisade mesophyll cells remain poorly understood despite their presence in diverse taxa and the critical role of the palisade layer in leaf-light interactions and carbon assimilation. Using micro-computed tomography, 3D ray tracing simulations, and physiological experiments, we tested the interactions between palisade cell geometry, chloroplast localization, light directional quality, and leaf optical and photosynthetic performance in the model taxon Viburnum. Simulations showed that lobed cells shifted between absorptance- or transmittance-dominated states depending on chloroplast localization, irrespective of light directional quality. In contrast, columnar palisade optics were driven by light directional quality, with absorptance-dominated properties under diffuse light and transmittance-dominated properties under direct light, irrespective of chloroplast localization. Lobed palisade cells in planta were less densely packed yet more productive on a per cell basis than columnar palisade cells, resulting in interspecific conservation of maximum carbon assimilation rate per unit leaf tissue. For the Viburnum species studied, our results indicate a 'many-to-one' mapping of multiple palisade cell forms to a common rate of photosynthetic productivity per unit tissue. This work highlights the dynamic relationship between palisade mesophyll form and function and informs the anatomical basis of plant carbon assimilation.
期刊介绍:
Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research.
As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.