• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

矿物质积累、相对含水量和气体交换是大麦应对盐胁迫的主要生理调节机制。

Mineral accumulation, relative water content and gas exchange are the main physiological regulating mechanisms to cope with salt stress in barley.

机构信息

Drylands and Oases Cropping Laboratory LACO, Institute of Arid Lands of Medenine (IRA), Sreet El Djorf 22.5 km, 4119, Medenine, Tunisia.

Department of Rural Engineering, Water, and Forests GREF, National Institute of Agronomic Research of Tunis (INAT), 43 Charles Nicolle, 1082, Tunis, Tunisia.

出版信息

Sci Rep. 2024 Jun 28;14(1):14931. doi: 10.1038/s41598-024-65967-5.

DOI:10.1038/s41598-024-65967-5
PMID:38942909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11213892/
Abstract

Salinity has become a major environmental concern for agricultural lands, leading to decreased crop yields. Hence, plant biology experts aim to genetically improve barley's adaptation to salinity stress by deeply studying the effects of salt stress and the responses of barley to this stress. In this context, our study aims to explore the variation in physiological and biochemical responses of five Tunisian spring barley genotypes to salt stress during the heading phase. Two salinity treatments were induced by using 100 mM NaCl (T1) and 250 mM NaCl (T2) in the irrigation water. Significant phenotypic variations were detected among the genotypes in response to salt stress. Plants exposed to 250 mM of NaCl showed an important decline in all studied physiological parameters namely, gas exchange, ions concentration and relative water content RWC. The observed decreases in concentrations ranged from, approximately, 6.64% to 40.76% for K, 5.91% to 43.67% for Na, 14.12% to 52.38% for Ca, and 15.22% to 38.48% for Mg across the different genotypes and salt stress levels. However, under salinity conditions, proline and soluble sugars increased for all genotypes with an average increase of 1.6 times in proline concentrations and 1.4 times in soluble sugars concentration. Furthermore, MDA levels rose also for all genotypes, with the biggest rise in Lemsi genotype (114.27% of increase compared to control). Ardhaoui and Rihane showed higher photosynthetic activity compared to the other genotypes across all treatments. The stepwise regression approach identified potassium content, K/Na ratio, relative water content, stomatal conductance and SPAD measurement as predominant traits for thousand kernel weight (R2 = 84.06), suggesting their significant role in alleviating salt stress in barley. Overall, at heading stage, salt accumulation in irrigated soils with saline water significantly influences the growth of barley by influencing gas exchange parameters, mineral composition and water content, in a genotype-dependent manner. These results will serve on elucidating the genetic mechanisms underlying these variations to facilitate targeted improvements in barley's tolerance to salt stress.

摘要

盐度已成为农业用地的主要环境问题,导致作物产量下降。因此,植物生物学专家旨在通过深入研究盐胁迫对大麦的影响以及大麦对这种胁迫的反应,从遗传学上提高大麦对盐度胁迫的适应能力。在这种情况下,我们的研究旨在探讨 5 个突尼斯春大麦基因型在抽穗期对盐胁迫的生理生化响应的变化。在灌溉水中用 100 mM NaCl(T1)和 250 mM NaCl(T2)诱导两种盐度处理。发现基因型对盐胁迫的响应存在显著的表型变异。暴露在 250 mM NaCl 下的植物所有研究的生理参数均显着下降,即气体交换、离子浓度和相对水含量(RWC)。观察到的浓度下降范围从不同基因型和盐胁迫水平的 K 浓度的约 6.64%至 40.76%、Na 浓度的 5.91%至 43.67%、Ca 浓度的 14.12%至 52.38%和 Mg 浓度的 15.22%至 38.48%。然而,在盐胁迫条件下,所有基因型的脯氨酸和可溶性糖含量均增加,脯氨酸浓度平均增加 1.6 倍,可溶性糖浓度增加 1.4 倍。此外,所有基因型的 MDA 水平也升高,其中 Lemsi 基因型的增幅最大(与对照相比增加 114.27%)。在所有处理中,Ardhaoui 和 Rihane 与其他基因型相比表现出更高的光合作用活性。逐步回归方法确定钾含量、K/Na 比、相对水含量、气孔导度和 SPAD 测量是千粒重的主要性状(R2=84.06),表明它们在缓解大麦盐胁迫方面具有重要作用。总的来说,在抽穗期,用盐水灌溉土壤中的盐分积累会通过影响气体交换参数、矿物质组成和含水量,以基因型依赖的方式显著影响大麦的生长。这些结果将有助于阐明这些变化背后的遗传机制,从而促进大麦对盐胁迫的耐受性的针对性提高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/92bf80242384/41598_2024_65967_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/9617a374341e/41598_2024_65967_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/ecf5df3604bc/41598_2024_65967_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/721e900d9cf2/41598_2024_65967_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/fb9ae6dfe58c/41598_2024_65967_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/3fc61f3e4704/41598_2024_65967_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/77ac8a6cd2c7/41598_2024_65967_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/6d06b92d9283/41598_2024_65967_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/3e4c34cefd8f/41598_2024_65967_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/583ffe38e426/41598_2024_65967_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/92bf80242384/41598_2024_65967_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/9617a374341e/41598_2024_65967_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/ecf5df3604bc/41598_2024_65967_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/721e900d9cf2/41598_2024_65967_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/fb9ae6dfe58c/41598_2024_65967_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/3fc61f3e4704/41598_2024_65967_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/77ac8a6cd2c7/41598_2024_65967_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/6d06b92d9283/41598_2024_65967_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/3e4c34cefd8f/41598_2024_65967_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/583ffe38e426/41598_2024_65967_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53aa/11213892/92bf80242384/41598_2024_65967_Fig10_HTML.jpg

相似文献

1
Mineral accumulation, relative water content and gas exchange are the main physiological regulating mechanisms to cope with salt stress in barley.矿物质积累、相对含水量和气体交换是大麦应对盐胁迫的主要生理调节机制。
Sci Rep. 2024 Jun 28;14(1):14931. doi: 10.1038/s41598-024-65967-5.
2
Additive effects of Na+ and Cl- ions on barley growth under salinity stress.钠离子和氯离子在盐胁迫下对大麦生长的累加效应。
J Exp Bot. 2011 Mar;62(6):2189-203. doi: 10.1093/jxb/erq422. Epub 2011 Jan 27.
3
Stomatal traits as a determinant of superior salinity tolerance in wild barley.气孔特征决定野生大麦的耐盐性优势。
J Plant Physiol. 2020 Feb;245:153108. doi: 10.1016/j.jplph.2019.153108. Epub 2019 Dec 28.
4
Genetic Variation and Alleviation of Salinity Stress in Barley ( L.).大麦( L.)遗传变异与耐盐性缓解。
Molecules. 2018 Sep 28;23(10):2488. doi: 10.3390/molecules23102488.
5
Interaction of salinity and cadmium stresses on mineral nutrients, sodium, and cadmium accumulation in four barley genotypes.盐分和镉胁迫对四种大麦基因型中矿质养分、钠和镉积累的交互作用。
J Zhejiang Univ Sci B. 2007 Jul;8(7):476-85. doi: 10.1631/jzus.2007.B0476.
6
Compatible solute accumulation and stress-mitigating effects in barley genotypes contrasting in their salt tolerance.耐盐性不同的大麦基因型中相容性溶质的积累及应激缓解效应
J Exp Bot. 2007;58(15-16):4245-55. doi: 10.1093/jxb/erm284.
7
Agro-morphological, biochemical, and molecular markers of barley genotypes grown under salinity stress conditions.在盐胁迫条件下生长的大麦基因型的农艺形态、生化和分子标记。
BMC Plant Biol. 2023 Oct 30;23(1):526. doi: 10.1186/s12870-023-04550-y.
8
Leaf water relations and net gas exchange responses of salinized Carrizo citrange seedlings during drought stress and recovery.干旱胁迫及恢复过程中盐渍化卡里佐枳橙幼苗的叶片水分关系和净气体交换响应
Ann Bot. 2007 Aug;100(2):335-45. doi: 10.1093/aob/mcm113. Epub 2007 Jun 15.
9
Stomatal and non-stomatal limitations are responsible in down-regulation of photosynthesis in melon plants grown under the saline condition: Application of carbon isotope discrimination as a reliable proxy.在盐胁迫条件下生长的甜瓜植物中,气孔和非气孔限制是光合作用下调的原因:碳同位素分馏作为可靠指标的应用。
Plant Physiol Biochem. 2019 Aug;141:1-19. doi: 10.1016/j.plaphy.2019.05.010. Epub 2019 May 15.
10
The proteome response of salt-resistant and salt-sensitive barley genotypes to long-term salinity stress.耐盐和盐敏感大麦基因型对长期盐胁迫的蛋白质组响应。
Mol Biol Rep. 2012 May;39(5):6387-97. doi: 10.1007/s11033-012-1460-z.

引用本文的文献

1
Evaluating the Necessity of a Control Treatment for Assessing Salt Tolerance in Wheat Genotypes Based on Agro-Physiological Traits in Real-Field Conditions.基于田间实际条件下的农业生理性状评估小麦基因型耐盐性时对照处理的必要性
Plants (Basel). 2025 Aug 11;14(16):2488. doi: 10.3390/plants14162488.
2
Bifunctional Phyto-Synthesized Nano Silver for Mitigating Salinity-Induced Dormancy and Associated Fungal Infections During Seed Germination in Brassica juncea with Integration of Machine Learning-Based Predictive Modeling.双功能植物合成纳米银用于缓解芥菜种子萌发期间盐分诱导的休眠及相关真菌感染,并结合基于机器学习的预测模型
Appl Biochem Biotechnol. 2025 Jul 7. doi: 10.1007/s12010-025-05301-5.
3

本文引用的文献

1
GO nanoparticles mitigate the negative effects of salt and alkalinity stress by enhancing gas exchange and photosynthetic efficiency of strawberry plants.GO 纳米粒子通过增强草莓植物的气体交换和光合作用效率来减轻盐和碱胁迫的负面影响。
Sci Rep. 2023 May 25;13(1):8457. doi: 10.1038/s41598-023-35725-0.
2
Physiological and biochemical changes in Moroccan barley ( L.) cultivars submitted to drought stress.遭受干旱胁迫的摩洛哥大麦(L.)品种的生理生化变化
Heliyon. 2023 Feb 10;9(2):e13643. doi: 10.1016/j.heliyon.2023.e13643. eCollection 2023 Feb.
3
Influence of Foliar Application of Hydrogen Peroxide on Gas Exchange, Photochemical Efficiency, and Growth of Soursop under Salt Stress.
Effects of exogenous chitosan concentrations on photosynthesis and functional physiological traits of hibiscus under salt stress.
外源壳聚糖浓度对盐胁迫下木槿光合作用及功能生理特性的影响
BMC Plant Biol. 2025 Apr 3;25(1):419. doi: 10.1186/s12870-025-06424-x.
4
Enhancing salinity tolerance in cultivated rice through introgression of African rice genes and application of moringa leaf extract.通过导入非洲稻基因和施用辣木叶提取物提高栽培稻的耐盐性。
BMC Plant Biol. 2025 Feb 7;25(1):163. doi: 10.1186/s12870-025-06102-y.
5
Enhancing Crop Resilience: The Role of Plant Genetics, Transcription Factors, and Next-Generation Sequencing in Addressing Salt Stress.增强作物抗逆性:植物遗传学、转录因子及新一代测序技术在应对盐胁迫中的作用
Int J Mol Sci. 2024 Nov 22;25(23):12537. doi: 10.3390/ijms252312537.
叶面喷施过氧化氢对盐胁迫下番荔枝气体交换、光化学效率及生长的影响
Plants (Basel). 2023 Jan 29;12(3):599. doi: 10.3390/plants12030599.
4
Assessment of proline function in higher plants under extreme temperatures.极端温度下高等植物中脯氨酸功能的评估
Plant Biol (Stuttg). 2023 Apr;25(3):379-395. doi: 10.1111/plb.13510. Epub 2023 Feb 27.
5
Effect of Salinity on Stomatal Conductance, Leaf Hydraulic Conductance, HvPIP2 Aquaporin, and Abscisic Acid Abundance in Barley Leaf Cells.盐度对大麦叶片细胞的气孔导度、叶片水力导率、HvPIP2 水通道蛋白和脱落酸含量的影响。
Int J Mol Sci. 2022 Nov 18;23(22):14282. doi: 10.3390/ijms232214282.
6
Physiological and Molecular Responses of Barley Genotypes to Salinity Stress.大麦基因型对盐胁迫的生理和分子响应。
Genes (Basel). 2022 Nov 5;13(11):2040. doi: 10.3390/genes13112040.
7
How salt stress-responsive proteins regulate plant adaptation to saline conditions.盐胁迫响应蛋白如何调节植物适应盐渍条件。
Plant Mol Biol. 2022 Feb;108(3):175-224. doi: 10.1007/s11103-021-01232-x. Epub 2021 Dec 29.
8
Proline, a multifaceted signalling molecule in plant responses to abiotic stress: understanding the physiological mechanisms.脯氨酸,一种在植物应对非生物胁迫反应中的多功能信号分子:理解其生理机制。
Plant Biol (Stuttg). 2022 Mar;24(2):227-239. doi: 10.1111/plb.13363. Epub 2021 Nov 18.
9
Foliar application of ascorbic acid enhances salinity stress tolerance in barley ( L.) through modulation of morpho-physio-biochemical attributes, ions uptake, osmo-protectants and stress response genes expression.叶面喷施抗坏血酸可通过调节形态生理生化特性、离子吸收、渗透保护剂和胁迫响应基因表达来增强大麦对盐胁迫的耐受性。
Saudi J Biol Sci. 2021 Aug;28(8):4276-4290. doi: 10.1016/j.sjbs.2021.03.045. Epub 2021 Mar 21.
10
Salinity Stress Affects Photosynthesis, Malondialdehyde Formation, and Proline Content in L.盐胁迫影响番茄中的光合作用、丙二醛形成和脯氨酸含量
Plants (Basel). 2021 Apr 22;10(5):845. doi: 10.3390/plants10050845.