Lunar magnetism impairs wheat seedling photosynthesis: A simulated environment study

IF 6.1 2区 生物学 Q1 PLANT SCIENCES
Jingkai Tang , Zizhou Wu , Zhiyin Sun , Hui Liu , Hong Liu
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引用次数: 0

Abstract

Plants evolved under Earth's stable geomagnetic field (GMF), a condition sharply contrasting with the near-absence of a global magnetic field on the Moon. However, the effects of this stark magnetic disparity on fundamental plant processes like photosynthesis remain underexplored, particularly in the context of future lunar agriculture. This study rigorously investigated the physiological and biochemical mechanisms underpinning the photosynthetic response of wheat seedlings – a staple crop selected for its centrality in closed-loop life support – to a simulated lunar weak magnetic field (WMF, <5 nT). We used a controlled environment and simulated lunar soil to compare wheat seedlings grown under precisely controlled WMF and GMF conditions. Our findings reveal that WMF significantly impeded seedling growth, as evidenced by diminished height, reduced hydration, and lower biomass accumulation. Photosynthetic gas exchange was severely compromised under WMF, manifesting as reduced net photosynthetic rate, stomatal conductance, and intercellular CO2 concentration. Light and CO2 response curve analyses further revealed a fundamental reduction in photosynthetic efficiency, characterized by lower apparent quantum efficiency and maximum photosynthetic capacity. Concomitantly, levels of key photosynthetic pigments (chlorophyll a, chlorophyll b, carotenoids) and ferritin were significantly depressed in WMF-exposed seedlings, suggesting a mechanistic link to impaired photosynthetic machinery and potentially compromised nutrient uptake. This inhibitory effect of lunar-level magnetic fields on photosynthetic carbon assimilation is likely mediated by disruptions in light energy conversion, electron transport chain efficiency, and RuBP regeneration capacity. Furthermore, the observed reduction in ferritin, a crucial iron storage protein, may exacerbate oxidative stress and limit iron availability for chlorophyll biosynthesis. These combined disruptions indicate a significant constraint on plant productivity in lunar environments, thereby limiting the viability of purely terrestrial-adapted crops for lunar agriculture. These findings underscore the need to consider magnetic field mitigation strategies or genetically adapt crops for optimal photosynthetic function in weak magnetic field environments to ensure sustainable plant-based life support beyond Earth. This research provides a vital foundation for future investigations into plant magneto-biology and the development of robust agricultural systems for space exploration.
月球磁场对小麦幼苗光合作用的影响:模拟环境研究
植物在地球稳定的地磁场(GMF)下进化,这与月球上几乎没有全球磁场形成鲜明对比。然而,这种明显的磁场差异对光合作用等基本植物过程的影响仍未得到充分探索,特别是在未来月球农业的背景下。本研究严格调查了小麦幼苗(一种主要作物,因其在闭环生命支持中处于中心位置而被选中)对模拟月球弱磁场(WMF, < 5nt)光合反应的生理和生化机制。我们利用受控环境和模拟月球土壤,比较了在精确控制的WMF和GMF条件下生长的小麦幼苗。我们的研究结果表明,WMF显著阻碍了幼苗的生长,表现为幼苗高度降低、水化减少和生物量积累减少。光合气体交换在WMF下受到严重损害,表现为净光合速率、气孔导度和胞间CO2浓度降低。光和CO2响应曲线分析进一步揭示了光合效率的根本降低,其特征是表观量子效率和最大光合能力降低。同时,在wmf暴露的幼苗中,关键光合色素(叶绿素a、叶绿素b、类胡萝卜素)和铁蛋白的水平显著降低,表明这与光合机制受损和潜在的营养吸收受损有机制联系。月球水平磁场对光合碳同化的抑制作用可能是由光能转换、电子传递链效率和RuBP再生能力的中断介导的。此外,铁蛋白(一种重要的铁储存蛋白)的减少可能会加剧氧化应激,限制叶绿素生物合成的铁可用性。这些综合破坏表明,在月球环境中,植物生产力受到严重限制,从而限制了纯粹适应陆地的月球农业作物的生存能力。这些发现强调有必要考虑磁场缓解策略或对作物进行基因改造,使其在弱磁场环境中发挥最佳的光合作用,以确保地球以外可持续的植物生命支持。这项研究为未来植物磁生物学的研究和空间探索农业系统的发展提供了重要的基础。
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来源期刊
Plant Physiology and Biochemistry
Plant Physiology and Biochemistry 生物-植物科学
CiteScore
11.10
自引率
3.10%
发文量
410
审稿时长
33 days
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.
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